Title of Invention	MULTIVALENT MEN INGOCOCCAL DERIVATIZED POLYSACCHARIDE-PROTEIN CONJUGATES AND VACCINE
Abstract	The present invention describes derivatized polysaccharide-protein conjugates, a composition comprising one or more of such derivatized polysaccharide-protein conjugates and methods of immunizing human pateints with the same. The derivatized

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FORM 2 THE PATENT ACT 1970 (39 of 1970) & The Patents Rules, 2003 COMPLETE SPECIFICATION (See section 10 and rule 13) 1. MULTIVALENT MENINGOCOCCAL DERIVATIZED POLYSACCHARIDE-PROTEIN CONJUGATES AND VACCINE 2.(A) AVENTIS PASTEURJNC. (B) UNITED STATE OF AMERICA (QDiscovery Drive,Swiftwater, PA 18370, UNITED STATE OF AMERICA The following specification particularly describes the invention and the manner in which it is to be performed. 1 BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to the field of medicine generally, and more specifically to microbiology, immunology, vaccines and the prevention of infection by a bacterial pathogen by immunization. 2. Summary of the Related Art Neisseria meningitidis is a leading cause of bacterial meningitis and sepsis throughout the world. The incidence of endemic meningococcal disease during the last thirty years ranges from 1 to 5 per 100,000 in the developed world, and from 10 to 25 per 100,000 in developing countries (Reido, F. X., et al., (1995) Ped. Infect. Pis. J. 14, pp.643-657). During epidemics the incidence of meningococcal disease approaches 1000 per 1000,000. There are approximately 2,600 cases of bacterial meningitis per year in the United States, and on average 330,000 cases in developing countries. The case fatality rate ranges between 10 and 20%. Pathogenic meningoacocci are enveloped by a polysaccharide capsule that is attached to the outer membrane surface of the organism. Thirteen different serogroups of meningococci have been identified on the basis of the immunological specificity of the capsular polysaccharide (Frasch, C. E., et al, (1985) Rev. Infect. Pis. 7, pp. 504-510). Of these thirteen serogroups, five cause the majority of meningococcal disease; these include serogroups A, B, C, W135, and Y. Serogroup A is responsible for most epidemic disease. Serogroups B, C, and Y cause the majority of endemic disease and localized outbreaks. 2 The human naso-oropharyngeal mucosa is the only known natural reservoir of Neisseria meningitidis. Colonization takes place both at the exterior surface of the mucosal cell and the subepithelial tissue of the nasopharynx. Carriage of meningococci can last for months. Spreading of meningococci occurs by direct contact or via air droplets. Meningococci become invasive by passing through the mucosal epithelium via phagocytic vacuoles as a result of endocytosis. Host defense of invasive meningococci is dependent upon complement-mediated bacteriolysis. The serum antibodies that are responsible for complement-mediated bacteriolysis are directed in large part against the outer capsular polysaccharide. Vaccines based on meningococcal polysaccharide have been described which elicit an immune response against the capsular polysaccharide. These antibodies are capable of complement-mediated bacteriolysis of the serogroup specific meningococci. The meningococcal polysaccharide vaccines are shown to be efficacious in children and adults (Peltola, H., et al., (1997) New Engl. J. Med 297, pp. 686-691 and Artenstein, M. S., et al., (1970) New Engl. J. Med. 282, pp. 417-420), but the efficacy is limited in infants and young children (Reingold, A. L., et al., (1985) Lancet 2, pp. 114-118). Subsequent doses of the polysaccharide in younger populations elicited a weak or no booster response (Goldschneidera, I., et al, (1973) J. Infect. Diseases 128. pp. 769-776 and Gold, R., et al., (1977) J. Infect. Diseases. 136, S31-S35). The duration of protection elicited by the meningococcal polysaccharide vaccines is not long lasting, and has been estimated to be between 3 to 5 years in adults and children above four years of age (Brandt, B. L. and Artenstein, M. S. (1975) J. Infect. Diseases. 131, pp. S69-S72, Kyhty, H., et al., (1980) J. Infect. Diseases. 142, pp. 861-868, and Cessey, S. J., et al., (1993) J. Infect. Diseases. 167, pp 1212-1216). For children from one to four years old the duration of protection is less than three years (Reingold, A. L., et al., (1985) Lancet 2, pp. 114-118). Polysaccharides are incapable of binding to the major histocompatibility complex molecules, a prerequisite for antigen presentation to and stimulation of T-helper lymphocytes, i.e., they are T-cell independent antigens. Polysaccharides are able to stimulate B lymphocytes for antibody production without the help of T-helper lymphocytes. As a result of the T-independent stimulation of the B lymphocytes, there is a lack of memory induction following immunization by these antigens. The polysaccharide antigens 3 are capable of eliciting very effective T-independent responses in adults, but these T-independent responses are weak in the immature immune system of infants and young children. T-independent polysaccharide antigens can be converted to T-dependent antigens by covalent attachment of the polysaccharides to protein molecules ("carriers" or "carrier proteins"). B cells that bind the polysaccharide component of the conjugate vaccine can be activated by helper T cells specific for peptides that are a part of the conjugated carrier protein. The T-helper response to the carrier protein serves to augment the antibody production to the polysaccharide. The serogroup B polysaccharide has been shown to be poorly to non-immunogenic in the human population (Wyle, F. A., et al., (1972) J. Infect. Diseases. 126, pp. 514-522). Chemical attachment of this serogroup polysaccharide to proteins has not significantly altered the immune response in laboratory animals (Jennings, H. J. and Lugowski, C. (1981) J. Immunol. 127, pp. 1011-1018). The reason for the lack of immune response to this serogroup polysaccharide is thought to arise from structural similarities between the serogroup B polysaccharide and polysialylateda host glycoproteins, such as the neural cell adhesion molecules. A meningococcal conjugate vaccine based on serogroup C polysaccharide has been described. This monovalent vaccine elicits a strong functional antibody response to the capsular polysaccharide present on strains of N. meningitidis corresponding to serogroup C. Such a vaccine is only capable of protecting against disease caused by serogroup C bacteria. Existing vaccines based on meningococcal polysaccharide are of limited use in young children and do not provide long-lasting protection in adults. The only meningococcal vaccine which as been shown to be capable of eliciting long-lasting protection in all groups, including children, at risk for meningococcal infection is based on a polysaccharide from a single serogroup of N. meningitidis and provides no protection against infection by other serogroups. Thus, a need exists for a meningococcal conjugate vaccine capable of conferring broad, long-lived protection against meningococcal disease in children and adults at risk for meningococcal infection. The multivalent meningococcal polysaccharides of the 4 present invention solve this need by providing vaccine formulations in which immunogenic polysaccharides from the major pathogenic serogroups of N. meningitidis have been converted to T-dependent antigens through conjugations to carrier proteins. FDA licensure of vaccines for meningococcal polysaccharides has been based on bactericidal assays with baby rabbit complement (SBA-BR) performed on blood samples of those immunized with the licensed vaccine. A number of government and expert panels have published current requirements and recommendations for assessing meningococcal polysaccharide vaccines on such assays, for example, WHO Expert Committee on Biological Standardization for demonstrating the induction of bactericidal antibody production in healthy adult subjects immunized with meningococcal vaccines against Neisseria meningitides serogroups A and C (WHO 1976); CDC SBA-BR in an international comparison study to establish the parameters for standardization of the assay uses the same standard reference serum, CDC donor R21654-3430107, that is one of the Quality Control serum samples in the comparison study (Maslanka SE, et al, 1997. Clin. Diaen. Lab. Immunol. 4:156-167); and the standardized CDC method, recommended by the WHO Expert Committee of the Department of Vaccines and Biologicals as the optimal methodology (WHO 1999). Licensure is granted because human immunity to meningococcal disease has been shown to correlate well with the level of complement-mediated bactericidal antibody detected by the Serum Bactericidal Assay (SBA) (Goldschneider, I, et al., 1969, J. Exp. Med. 129:1307-1326 and Goldschneider, I, et al., 1969, J. Exp. Med. 129:1327-1348). A surrogate level of a 1:4 SBA titer against serogroup C has been established using a human complement in the assay (SBA-H). However, licensing requirements for meningococcal polysaccharide vaccines are based on the induction of serum bactericidal responses using baby rabbit complement (SBA-BR) as the source of complement in the assay (World Health Organization. 1976. Requirements for meningococcal polysaccharide vaccine. World Health Organization technical report series, no. 594. World Health Organization, Geneva, Switzerland (WHO 1976). According to this recommendation, the antibody titers of the sera from at least 90% of subjects vaccinated with meningococcal polysaccharide vaccine should show a 4-fold or greater rise 2-4 weeks after immunization when tested against the 5 following target strains or equivalent strains: Al for serogroup A, CI 1 for serogroup C, S-1975 for serogroup Y, and S-4383 for serogroup W-135 (WHO 1976, WHO 1981, Bureau of Biologies, Food and Drug Administration July 17,1985). The Bureau of Biologies adopted the WHO recommendation and the meningococcal polysaccharide vaccines, groups A and C combined and groups A, C, Y, and W-135 combined, are licensed in the United States based upon this requirement. In order to facilitate interlaboratory comparisons of the bactericidal activity induced by meningococcal vaccines, a standardized SBA using baby rabbit complement (SBA-BR) is established through a multilaboratory study (Maslanka SE, et al., 1997. Clin. Diaen. Lab. Immunol. 4:156-167. As data from meningococcal conjugate C vaccines started to become available, concerns began to emerge that the use of rabbit complement in the assay may lead to falsely high SBA titers. Following a March 1999 meeting to clarify and resolve issues relating to the laboratory assay for the analysis of human serum for meningococcal serogroups A and C specific antibodies, the WHO Expert Committee on Biological Standardization recommended that the SBA with baby rabbit complement be used for measuring antibody responses to serogroup C (The World Health Organization. 1999. Standardization and validation of serological assays for the evaluation of immune responses to Neisseria meningitidis serogroup A/C vaccines. Geneva, WHO/V&B/99.19 (WHO 1999)). In an effort to avoid overestimating protection using baby rabbit complement, the WHO recommended that a study be undertaken to correlate the threshold titers measured by the SBA assay using baby rabbit complement relative to SBA titers measured using human complement. A follow-up meeting is held and results presented to support a general conclusion that a SBA titer of =1:128 using baby rabbit complement correlates well to the protective SBA titer of 1:4 using human complement. No information is provided for corresponding correlate SBA-BR titers, for other meningococcal serogroups, such as A, Y or W-135 or for polysaccharide conjugates. SBA titers between 1:8 and 1:64 using baby rabbit complement do not necessarily correlate well with the protective SBA titer of 1:4 using human complement (Jodar L, et al., Biologicals 2002; 30: 323-329). The WHO Expert Committee recommended that post 6 vaccination SBA-BR titers of 1:8,1:16,1:32 and 1:64 be reassessed using human complement. Other measures to resolve the uncertainties of the SBA-BR titers of 1:8, 1:16,1:32, and 1:64 included the assessment of four-fold rise in antibody SBA titers between pre-and post-vaccination. Demonstration of memory as a correlate of protection is also offered, however the Expert Committee recognized that the available data for these surrogates are either inadequate or limited. An SBA-BR titer higher than 1:8 is a better indicia of human immunity to meningococcal disease, as is a four-fold rise or higher, of SBA-BR titer from pre-immunization to post-10 immunization period of about 15 to about 45 days after immunization. In one embodiment, the present invention provides a method of immunizing a human patient with a multivalent meningococcal polysaccharide conjugate composition, wherein the human patient has a serum SBA-BR titer of 1:16 or higher, preferably, of 1:32 or higher, and more preferably, 1:64 or higher, and even more preferably, 1:128 or higher. In still further embodiments, the present invention provides a method of immunizing a human patient with a meningococcal polysaccharide conjugate composition, wherein the human patient has four-fold rise, or higher, in antibody SBA titers between pre- and post-vaccination. In still another embodiment, the present invention provides a method of providing immunity to a human patient against multiple serogroups of N. meningococcal by immunizing the human patient with a multivalent meningococcal polysaccharide conjugate composition, wherein the composition comprises two or more polysaccharides selected from N. meningococcal serogroups A and W-135; Y and W-135; C and Y; C and W-135; A,C and Y; A,C and W-135; C,Y and W-135; A,Y and W-135; and A,C,Y and W-135. In still further embodiments, the present invention provides a method of providing immunity to a human patient against multiple serogroups of N. meningococcal and by immunizing the human patient with a multivalent meningococcal (purified) polysaccharide conjugate composition, wherein the polysaccharide is derivatized to less than 100,000 daltons. In one embodiment of the invention, the purified polysaccharide is depolymerized to an average polysaccharide size of about 5,000 to about 75,000 daltons; preferably, to an 7 average polysaccharide size of about 7,000 to about 50,000 daltons; more preferably, to an average polysaccharide size of about 8,000 to about 35,000 daltons; even more preferably, to an average polysaccharide size of about 12,000 to about 25,000 daltons. In one embodiment of the invention, the average polysaccharide size in the composition is about 15,000 to about 22,000 daltons. SUMMARY OF THE INVENTION The present invention provides a method of providing human immunity to meningococcal disease caused by pathogenic Neisseria meningitidis by administration of immunological 10 compositions of meningococcal polysaccharide-protein conjugates. In one embodiment of the invention, the immunological composition comprises two or more protein-polysaccharide conjugates, wherein each of the conjugates comprises a capsular polysaccharide from N. meningitidis conjugated to a carrier protein. In a preferred embodiment, the immunological composition comprises two or more distinct protein-polysaccharide conjugates, wherein each of the conjugates comprises a, capsular polysaccharide from a different serogroup of N. meningitidis conjugated to a carrier protein. The present invention provides a method of providing human immunity to meningococcal disease caused by pathogenic Neisseria meningitidis comprising administration of an immunological composition comprising two or more distinct protein-polysaccharide conjugates, wherein each of the conjugates comprises a capsular polysaccharide from a different serogroup of N. meningitidis conjugated to a carrier protein. The present invention provides a method of providing human immunity to meningococcal disease caused by pathogenic Neisseria meningitidis comprising administration of meningococcal polysaccharide-protein conjugates. The present invention provides multivalent meningococcal vaccines comprised of immunologically effective amounts of from two to four distinct protein-polysaccharide conjugates, wherein each of the conjugates contains a different capsular polysaccharide conjugated to a carrier protein, and wherein each capsular polysaccharide is selected from the group consisting of capsular polysaccharide from serogroups A, C, W-135 and Y. The present invention further provides a method of inducing an immunological response to capsular polysaccharide of N. meningitidis comprising administering an immunologically effective amount of the 8 immunological composition of the invention to a human. In one embodiment, the multivalent meningococcal vaccine comprises immunologically effective amounts of two distinct protein-polysaccharide conjugates, wherein each of the conjugates contains a different capsular polysaccharide conjugated to a carrier protein, and wherein each capsular polysaccharide is selected from the group consisting of capsular polysaccharide from serogroups A, C, W-135 and Y, more preferably, comprises capsular polysaccharides A and W-135, A and Y, C and W-135, C and Y, and W-135 and Y. In one embodiment, the multivalent meningococcal vaccine comprises immunologically effective amounts of three distinct protein-polysaccharide conjugates, wherein each of the conjugates contains a different capsular polysaccharide conjugated to a carrier protein, and wherein each capsular polysaccharide is selected from the group consisting of capsular polysaccharide from serogroups A, C, W-135 and Y, more preferably, comprises capsular polysaccharides A, C and W-135, A, C and Y, C, Y and W-135, C, W-135 and Y, and A, W-135 and Y. In another embodiment, the multivalent meningococcal vaccine comprises immunologically effective amounts of four distinct protein-polysaccharide conjugates, wherein each of the conjugates contains a different capsular polysaccharide conjugated,to a carrier protein, and wherein each capsular polysaccharide is selected from the group consisting of capsular polysaccharide from serogroups A, C, W-135 and Y. The present invention further provides a method of inducing an immunological response to capsular polysaccharide of N. meningitidis comprising administering an immunologically effective amount of the immunological composition of the invention to a human or animal. The present invention provides a multivalent meningococcal vaccine comprised of immunologically effective amounts of from two to four distinct protein-polysaccharide conjugates, wherein each of the conjugates contains a different capsular polysaccharide conjugated to a carrier protein, and wherein each capsular polysaccharide is selected from the group consisting of capsular polysaccharide from serogroups A, C, W-135 and Y. The present invention provides a method of protecting a human or animal susceptible to infection from N. meningitidis comprising administering an immunologically effective dose of the vaccine of the invention to the human or animal. 9 All patents, patent applications, and other publications recited herein are hereby incorporated by reference in their entirety. DETAILED DESCMPTION OF THE INVENTION The present invention comprises an immunological composition pf two or more distinct protein-polysaccharide conjugates, wherein each of the conjugates comprises a capsular polysaccharide conjugated to a carrier protein. Thus, the present invention includes compositions that comprise two or more different derivatized capsular polysaccharides conjugated to one or more carrier protein(s). Capsular polysaccharides can be prepared by standard techniques known to those of skill in the art. In the present invention capsular polysaccharides prepared from serogroups A, C, W-135 and Y of N. meningitidis are preferred. In a preferred embodiment, these meningococcal serogroup conjugates are prepared by separate processes and formulated into a single dosage formulation. For example, capsular polysaccharides from serogroups A, C, W-135 and Y of N. meningitidis are separately purified. In a preferred embodiment of the present invention the purified polysaccharide is depolymerized and activated prior to conjugation to a carrier protein. In a preferred embodiment of the present invention capsular polysaccharides of serogroups A, C, W-135, and Y from N. meningitidis are partially depolymerized using mild oxidative conditions. Native meningococcal polysaccharide is about 500,000 to 1,500,000 daltons. The present invention is directed to meningococcal polysaccharides of a smaller size. When purifying native polysaccharides, a certain percentage of the polysaccharides will be of a smaller size. However, to obtain a better yield, it is generally preferred to depolymerize, or derivatize the native meningococcal polysaccharide to a preferred size range, preferably less than 100,000 daltons. In one embodiment of the invention, the purified polysaccharide is depolymerized to an average polysaccharide size of about 5,000 to about 75,000 daltons; preferably, to an average polysaccharide size of about 7,000 to about 50,000 daltons; more preferably, to an average polysaccharide size of about 8,000 to about 35,000 daltons; even more preferably, to an average polysaccharide size of about 12,000 to about 25,000 daltons. In one 10 embodiment of the invention, the average polysaccharide size in the composition is about 15,000 to about 22,000 daltons. The depolymerization or partial depolymerization of the polysaccharides may then be followed by an activation step. By "activation" is meant chemical treatment of the polysaccharide to provide chemical groups capable of reacting with the carrier protein. A preferred activation method involves treatment with adipic acid dihyrazide in physiological saline at pH 5.0.+-.0.1 for approximately two hours at 15 to 30 deg. C. One process for activation is described in U.S. Pat. No. 5,965,714. Once activated, the capsular polysaccharides may then be conjugated to one or more carrier proteins. In a preferred embodiment of the present invention each capsular polysaccharide is separately conjugated to a single carrier protein species. In a preferred embodiment the capsular polysaccharides from serogroups A, C, W-135 and Y of N. meningitidis are each separately conjugated to the same carrier protein species. Carrier proteins may include bacterial toxins such as diphtheria toxin, inactivated bacterial toxins such as diphtheria toxoid, CRM197, tetanus toxoid, pertussis toxoid, E. coli LT, E. coli ST, and exotoxin A from Pseudoinonas aeruginosa. Bacterial outer membrane proteins such as, outer membrane complex c (OMPC), porins, transferrin binding proteins, pneumolysis, pneumococcal surface protein A (PspA), or pneumococcal adhesin protein (PsaA), could also be used. Other proteins, such as ovalbumin, keyhole limpit hemocyanin bovine serum albumin (BSA) or purified protein derivative of tuberculin (PPD) may also be used as carrier proteins. Carrier proteins are preferably proteins that are non-toxic and non-reactogenic and obtainable in sufficient amount and purity. Carrier proteins should be amenable to standard conjugation procedures. In a preferred embodiment of the present invention diphtheria toxin purified from cultures of Corynebacteria diphtheriae and chemically detoxified using formaldehyde is used as the carrier protein. An alternative carrier protein is Protein D which is an outer membrane surface exposed protein of H. influenza. In one embodiment of the invention, the average ratio of each derivatized polysaccharide to carrier protein is about 1:1 to about 1:20 (w/w). In a preferred embodiment of the invention, the average ratio of total derivatized polysaccharide to carrier protein is about 1:2 11 to about 1:10 (w/w), and an even more preferred average ratio of each derivatized polysaccharide to carrier protein is about 1:2 to about 1:6 (w/w). In a more preferred embodiment of the invention, the average ratio of total derivatized polysaccharide to carrier protein is about 1:(4±1); more preferably, 1:(4A.5), even more preferably, 1:(4A.25) (w/w). After conjugation of the capsular polysaccharide to the carrier protein, the polysaccharide-protein conjugates may be purified (enriched with respect to the amount of polysaccharide-protein conjugate) by a variety of techniques. One goal of the purification step is to remove the unbound polysaccharide from the polysaccharide-protein conjugate. One method for purification, involving ultrafiltration in the presence of ammonium sulfate, is described in U.S. Pat. No. 6,146,902. Alternatively, conjugates can be purified away from unreacted protein and polysaccharide by any number of standard techniques including, inter alia, size exclusion chromatography, density gradient centrifugation, hydrophobic interaction chromatography or ammonium sulfate fractionation. See, e.g., P. W. Anderson, et. al. (1986). J. Immunol. 137:1181-1186. See also H. J. Jennings and C. Lugowski (1981) J. Immunol. 127: 1011-1018. After conjugation of the polysaccharide and carrier protein the immunological compositions of the present invention are made by combining the various derivatized polysaccharide-protein conjugates. The immunological compositions of the present invention comprise two or more different capsular polysaccharides conjugated to one or more carrier protein(s). A preferred embodiment of the present invention is a bivalent immunological composition comprising derivatized capsular polysaccharides from serogroups A and C of TV. meningitidis separately conjugated to diptheria toxin or toxoid. More preferably the present invention is a tetravalent immunological composition comprising capsular polysaccharides from serogroups A, C, W-135 and Y of N. meningitidis separately conjugated to diptheria toxin or toxoid. The present invention is directed, in part, to a composition of multicomponent, derivatized polysaccharide conjugates where each derivatized polysaccharide is present in about 0.5 to about 15 gg per dose. Thus, the composition may comprise a total derivatized polysaccharide gg of 1 gg to 60 ug. In a preferred embodiment, the relative amount of each 12 derivatized polysaccharide in the composition is about equal within ± 50%; more preferably, within ± 30%; even more preferably, within ± 20%. Preparation and use of carrier proteins, and a variety of potential conjugation procedures, are well known to those skilled in the art. Conjugates of the present invention can be prepared by such skilled persons using the teachings contained in the present invention as well as information readily available in the general literature. Guidance can also be obtained from any one or all of the following U.S. patents, the teachings of which are hereby incorporated in their entirety by reference: U.S. Pat. Nos. 4,356,170; 4,619,828; 5,153,312; 5,422,427 and 5,445,817. Alternatively, the immunological compositions may be made by either culturing two or more N. meningitidis serogroups together and copurifying, depolymerizing, activating and conjugating the polysaccharides, or by culturing purifying the N. meningitidis serogroups separately and combining two or more purified polysaccharides before or after any of the steps of depolymerizing, activating and conjugating the polysaccharides. The immunological compositions of the present invention are made by separately preparing polysaccharide-protein conjugates from different meningococcal serogroups and then combining the conjugates. The immunological compositions of the present invention can be used as vaccines. Formulation of the vaccines of the present invention can be accomplished using art recognized methods. The vaccine compositions of the present invention may also contain one or more adjuvants. Adjuvants include, by way of example and not limitation, aluminum adjuvants (e.g., aluminum salts such as aluminum hydroxide, aluminum phosphate, aluminum sulfate or combinations thereof), Freund"s Adjuvant (Complete or Incomplete), BAY, DC-chol, pcpp, monophoshoryl lipid A, CpG, QS-21, cholera toxin and formyl methionyl peptide. See, e.g., Vaccine Design, the Subunit and Adjuvant Approach, 1995 (M. F. Powell and M. J. Newman, eds., Plenum Press, N.Y.). The adjuvant is preferably an aluminum adjuvant, such as aluminum hydroxide or aluminum phosphate. Alternative adjuvants include oil-in-water emulsion formulations for example MF59 as described in PCT Publ. No. WO 90/14837); SAF, containing 10% Squalane, 0.4% Tween 80,5% pluronic-blocked polymer L121, and thr-MDP, RibiTM adjuvant system (RAS), (Ribi Immunochem, Hamilton, MT) containing 2% Squalene, 0.2% Tween 80, and one or 13 more bacterial cell wall components from the group consisting of monophosphorylipid A (MPL), trehalose dimycolate (TDM), and cell wall skeleton (CWS), preferably MPL+CWS (DetoxTM); saponin adjuvants, such as StimulonTM (Cambridge Bioscience, Worcester, Mass.) may be used or particles generated there from such as ISCOMs (immunostimulating complexes); cytokines, such as interleukins (e. g., IL-1, IL-2, IL-4, IL-5, IL-6, IL-7, IL-12, etc.), interferons (e.g., gamma interferon), macrophage colony stimulating factor (M-CSF), tumor necrosis factor (TNF). In one embodiment of the invention, the protein-polysaccharide conjugates have an average glycosylation ratio (polysaccharide to protein ratio) of about 0.05 to about 2; more preferably, an average ratio of about 0.08 to about 1.25; and even more preferably, an average ratio of about 0.1 to about 0.9. In one preferred embodiment, the protein-polysaccharide conjugates have an average glycosylation ratio polysaccharide to protein ratio of about 0.2 to about 0.8; more preferably, an average ratio of about 0.2 to about 0.6, and even more preferred embodiment, an average ratio of about 0.3 to about 0.5. As demonstrated below, the vaccines and immunological compositions according to the invention elicit a T-dependent-like immune response in various animal models, whereas the polysaccharide vaccine elicits a T-independent-like immune response. Thus, the compositions of the invention are also useful research tools for studying the biological pathways and processes involved in T-dependent-like immune responses to N. meningitidis antigens. The amount of vaccine of the invention to be administered a human or animal and the regime of administration can be determined in accordance with standard techniques well known to those of ordinary skill in the pharmaceutical and veterinary arts taking into consideration such factors as the particular antigen, the adjuvant (if present), the age, sex, weight, species and condition of the particular animal or patient, and the route of administration. In the present invention, the amount of polysaccharide-protein carrier to provide an efficacious dose for vaccination against AT. meningitidis can be from between about 0.02 ug to about 5 ug per kg body weight. In a preferred composition and method of the present invention the dosage is between about 0.1 ug to 3 ug per kg of body weight. For example, an efficacious dosage will require less antibody if the post-infection time elapsed is less since t h e is less time for the bacteria to proliferate. In like manner an efficacious 14 dosage will depend on the bacterial load at the time of diagnosis. Multiple injections administered over a period of days could be considered for therapeutic usage. The multivalent conjugates of the present invention can be administered as a single dose or in a series (i.e., with a "booster" or "boosters"). For example, a child could receive a single dose early in life, then be administered a booster dose up to ten years later, as is currently recommended for other vaccines to prevent childhood diseases. The booster dose will generate antibodies from primed B-cells, i.ei, an anamnestic response. That is, the multivalent conjugate vaccine elicits a high primary (i.e., following a single administration of vaccine) functional antibody response in younger populations when compared to the licensed polysaccharide vaccine, and is capable of eliciting an anamnestic response (i.e., following a booster administration), demonstrating that the protective immune response elicited by the multivalent conjugate vaccine of the present invention is long-lived. Compositions of the invention can include liquid preparations for orifice, e.g., oral, nasal, anal, vaginal, peroral, intragastric; mucosal (e.g., perlinqual, alveolar, gingival, olfactory or respiratory mucosa) etc., administration such as suspensions, syrups or elixirs; and, preparations for parenteral, subcutaneous, intradermal, intramuscular, intraperitoneal or intravenous administration (e.g., injectable administration), such as sterile suspensions or emulsions. Intravenous and parenteral administration are preferred. Such compositions may be in admixture with a suitable carrier, diluent, or excipient such as sterile water, physiological saline, glucose or the like. The compositions can also be lyophilized. The compositions can contain auxiliary substances such as wetting or emulsifying agents, pH buffering agents, gelling or viscosity enhancing additives, preservatives, flavoring agents, colors, and the like, depending upon the route of administration and the preparation desired. Standard texts, such as "REMINGTON"S PHARMACEUTICAL SCIENCE", 17.sup.th edition, 1985, incorporated herein by reference, may be consulted to prepare suitable preparations, without undue experimentation. In one embodiment of the invention, a preferred route of administration is intramuscular or subcutaneous, with intramuscular route preferred. Administration may be by injection or by an alternative delivery device. 15 Compositions of the invention are conveniently provided as liquid preparations, e.g., isotonic aqueous solutions, suspensions, emulsions or viscous compositions that may be buffered to a selected pH. If digestive tract absorption is preferred, compositions of the invention can be in the "solid" form of pills, tablets, capsules, caplets and the like, including "solid" preparations which are time-released or which have a liquid filling, e.g., gelatin covered liquid, whereby the gelatin is dissolved in the stomach for delivery to the gut. If nasal or respiratory (mucosal) administration is desired, compositions may be in a form and dispensed by a squeeze spray dispenser, pump dispenser or aerosol dispenser. Aerosols are usually under pressure by means of a hydrocarbon. Pump dispensers can preferably dispense a metered dose or a dose having a particular particle size. Liquid preparations are normally easier to prepare than gels, other viscous compositions, and solid compositions. Additionally, liquid compositions are somewhat more convenient to administer, especially by injection or orally, to animals, children, particularly small children, and others who may have difficulty swallowing a pill, tablet, capsule or the like, or in multi-dose situations. Viscous compositions, on the other hand, can be formulated within the appropriate viscosity range to provide longer contact periods with mucosa, such as the lining of the stomach or nasal mucosa. In a preferred embodiment of the invention, the vaccine composition is formulated as a sterile liquid, pyrogen-free, phosphate-buffered physiological saline, with or without a preservative. In one preferred embodiment, the formula per dose, comprises about 0.3 to about 1.0 mg sodium phosphate and about 3.5 to about 6.0 mg sodium chloride and up to 1.5 mL water. In one preferred embodiment, the formula per dose, comprises about 0.6 ± 0.2 mg sodium phosphate and 4.4 ± 0.2 mg sodium chloride and up to about 0.5 ± 0.2 mL water. Obviously, the choice of suitable carriers and other additives will depend on the exact route of administration and the nature of the particular dosage form, e.g., liquid dosage for (e.g., whether the composition is to be formulated into a solution, a suspension, gel or another liquid form), or solid dosage form (e.g., whether the composition is to be formulated into a pill, tablet, capsule, caplet, time release form or liquid-filled form). Solutions, suspensions and gels, normally contain a major amount of water (preferably 16 purified water) in addition to the active ingredient. Minor amounts of other ingredients such as pH adjusters (e.g., a base such as NaOH), emulsifiers or dispersing agents, buffering agents, preservatives, wetting agents, jelling agents, (e.g., methylcellulose), colors and/or flavors may also be present. The compositions can be isotonic, i.e., it can have the same osmotic pressure as blood and lacrimal fluid. The desired isotonicity of the compositions of this invention may be accomplished using sodium tartrate, propylene glycol or other inorganic or organic solutes. In one embodiment, the preferred isotonicity of the composition is obtained from sodium phosphate or sodium chloride, or mixtures thereof. Sodium chloride is preferred particularly for buffers containing sodium ions. Viscosity of the compositions may be maintained at the selected level using a pharmaceutically acceptable thickening agent. Methylcellulose is preferred because it is readily and economically available and is easy to work with. Other suitable thickening agents include, for example, xanthan gum, carboxymethyl cellulose, hydroxypropyl cellulose, carbomer, and the like. The preferred concentration of the thickener will depend upon the agent selected. The important point is to use an amount that will achieve the selected viscosity. Viscous compositions are normally prepared from solutions by the addition of such thickening agents. A pharmaceutically acceptable preservative can be employed to increase the shelf life of the compositions. Benzyl alcohol may be suitable, although a variety of preservatives including, for example, parabensa, thimerosal, chlorobutanol, or benzalkonium chloride may also be employed. A suitable concentration of the preservative will be from 0.02% to 2% based on the total weight although there may be appreciable variation depending upon the agent selected. Those skilled in the art will recognize that the components of the compositions must be 30 selected to be chemically inert with respect to the N. meningitidis polysaccharide-protein carrier conjugates. The invention will be further described by reference to the following illustrative, non- 17 limiting examples setting forth in detail several preferred embodiments of the inventive concept. Other examples of this invention will be apparent to those skilled in the art without departing from the spirit of the invention. The following abbreviations and Trademarks are: ACIP, Advisory Committee on Immunization Practices; AE, Adverse Event; Cetavalon™, cetyltrimethylammonium bromide, CTAB; CFR, Code of Federal Regulations; CRF, Case Report Form; DTP, Diphtheria Tetanus Pertussis; ELISA, Enzyme Linked Immunosorbent Assay; FDA, Food and Drug Administration; GCP, Good Clinical Practice; GMC, Geometric Mean Concentration; GMT, Geometric Mean Titer; IgG, Immunoglobulin G; IgGI, Immunoglobulin G subclass 1; IgG2, Immunoglobulin G subclass 2; IgM, Immunoglobulin M; ICH, International Conference on Harmonization; IND, Investigational New Drug; KB, Institutional Review Board; MenA/C-Dt Bivalent (A and C) Meningococcal Polysaccharide Diphtheria Conjugate Vaccine; MenPS, Meningococcal group specific polysaccharide; mL milliliter; Menomune1, licensed Meningococcal A,C Y and W-135 polysaccharide vaccine; OD, Optical Density; PBS, Phosphate Buffered Saline; SAE, Serious Adverse Event; SBA, Serum bactericidal activity; SBA-BR, Serum bactericidal activity assay performed using baby rabbit complement; SBA-HC, Serum bactericidal activity assay performed using human complement; SIDS, Sudden Infant Death Syndrome; TetraMenD, Tetravalent (A, C, Y, and W-135) Menmgococcal Polysaccharide Diphtheria Conjugate Vaccine; Td, Tetanus and Diphtheria vaccine; UAE, Unexpected Adverse Experience; URI, Upper Respiratory Infection; ug, Micrograms. EXAMPLES Example 1 Preparation of Neisseria meningitidis Serogroups A, C, W-135, and Y Purified Capsular Polysaccharides Powders Crude Paste Preparation Separately, Neisseria meningitidis serogroup A, C, W-135, and Y wet frozen seed cultures are thawed and recovered with the aid of liquid Watson Scherp medium and planted in Blake bottles containing Mueller Hinton agar medium. The Blake are incubated at 35 to 37 deg. C. in a C02 atmosphere for 15 to 19 hours. Following the incubation period, the growth from the Blake bottles are dislodged and added to 4 L flasks containing Watson Scherp 18 medium. The flasks are incubated at 35 to 37 deg. C. for 3 to 7 hours on a platform shaker. The contents of the 4 L flasks are transferred to a fermenter vessel containing Watson Scherp medium. The fermenter vessel is incubated at 35 to 37 deg. C. for 7 to 12 hours controlling dissolved oxygen content and pH with supplement feed and antifoam additions. After the incubation period, the contents of the fermentor vessel are transferred to a 500 L tank, Cetavlon is added, and the material mixed for 1 hours. The Cetavlon treated growth is centrifuged at approximately 15,000 to 17,000 x g at a flow rate of approximately 30 to 70 liters per hours. The crude polysaccharide is precipitated from the supernatant with a second Cetavlon precipitation. Cetavlon is added to the supernatant and the material mixed for at least 1 hour at room temperature. The material is stored at 1 to 5 deg. C. for 8 to 12 hours. The precipitated polysaccharide is collected centrifugation at approximately 45,000 to 50,000 x g at a flow rate of 300 to 400 ml per minute. The collected paste is stored at -60 deg. C. or lower until further processed. Purified Polysaccharide Powder Preparation The inactivated paste is thawed and transferred to a blender. The paste is blended with 0.9 M calcium chloride to yield a homogeneous suspension. The suspension is centrifuged at approximately 10,000 x g for 15 minutes. The supernatant is decanted; through a lint free pad into a container as the first extract. A second volume of 0.9 M calcium chloride is added to the paste, and blended to yield a homogeneous suspension. The suspension is centrifuged as above, and the supernatant combined with the supernatant from the first extraction. A total of four extractions are performed, and the supernatants pooled. The pooled extracts are concentrated by ultrafiltration using 10-30 kDa MWCO spiral would ultrafiltration units. Magnesium chloride is added to the concentrated, and the pH adjusted to 7.2 to 7.5 using sodium hydroxide. DNase and RNase are added to the concentrate, and incubated at 25 to 28 deg. C. with mixing for 4 hours. Ethanol is added to a concentration of 30 to 50%. Precipitated nucleic acid and protein are removed by centrifugation at 10,000 x g for 2 hours. The supernatant is recovered and the polysaccharide precipitated by adding ethanol to 80% and allowing it to stand overnight at 1 to 5 deg. C. The alcohol is siphoned off, and the precipitated polysaccharide is centrifuged for 5 minutes at 10,000 x g. The precipitated polysaccharide is washed with alcohol. The polysaccharide is washed with acetone, centrifuged at 15 to 20 minutes at 10,000 x g. The polysaccharide is dried under vacuum. 19 The initial polysaccharide powder is dissolved into sodium acetate solution. Magnesium chloride is added and the pH adjusted to 7.2 to 7.5 using sodium hydroxide solution. DNase and lZNase are added to the solution and incubated at 25 to 28 deg. C. with mixing for 4 hours to remove residual nucleic acids. After incubation with these enzymes, an equal volume of sodium acetate-phenol solution is added to the polysaccharide-enzyme mixture, and placed on a platform shaker at 1 to 5 deg. C. for approximately 30 minutes. The mixture is centrifuged at 10,000 x g for 15 to 20 minutes. The upper aqueous layer is recovered and saved. An equal volume of sodium acetate-phenol solution is added to the aqueous layer, and extracted as above. A total of four extractions are performed to remove protein and endotoxin from the polysaccharide solution. The combined aqueous extracts are diluted up to ten fold with water for injection, and diafiltered against 10 volumes"of water for injection. Calcium chloride is added to the diafiltered polysaccharide. The polysaccharide is precipitated overnight at 1 to 5 deg. C. by adding ethanol to 80%. The alcohol supernatant is withdrawn, and the polysaccharide collected by centrifugation at 10,000 x g for 15 minutes. The purified polysaccharide is washed two times with ethanol, and once with acetone. The washed powder is dried under vacuum in a desiccator. The dried powder is stored at -30 deg. C. or lower until processed onto conjugate. Example 2 Depolymerization of Neisseria meningitidis serogroups A,C, W135, and 20 Y Purified Capsular Polysaccharide Powder Materials used in the preparation include purified capsular polysaccharide powders from Neisseria meningitidis serogroups A, C, W-135, and Y (prepared in accordance with Example 1), sterile 50 mM sodium acetate buffer, pH 6.0, sterile IN hydrocholoric acid, sterile IN sodium hydroxide, 30% hydrogen peroxide, and sterile physiological saline (0.85% sodium chloride). Each serogroup polysaccharide is depolymerized in a separate reaction. A stainless steel tank is charged with up to 60 g of purified capsular polysaccharide powder. Sterile 50 mM sodium acetate buffer, pH 6.0 is added to the polysaccharide to yield a concentration of 2.5 g polysaccharide per liter. The polysaccharide solution is allowed to mix at 1 to 5 deg. C. for 12 to 24 hours to effect solution. The reaction tank is connected to a heat exchanger unit. Additional 50 mM sodium acetate buffer, pH 6.0, is added to dilute the polysaccharide to 20 reaction concentration of 1.25 g per liter. The polysaccharide solution is heated to 55 deg. C..+-.0.1. An aliquot of 30% hydrogen peroxide is added to the reaction mixture to yield a reaction concentration of 1% hydrogen peroxide. The course of the reaction is monitored by following the change in the molecular size of the polysaccharide over time. Every 15 to 20 minutes, aliquots are removed from the reaction mixture and injected onto a HPSEC column to measure the molecular size of the polysaccharide. When the molecular size of the polysaccharide reached the targeted molecular size, the heating unit is turned off and the polysaccharide solution rapidly cooled to 5 deg. C. by circulation through an ice water bath. The depolymerized polysaccharide solution is concentrated to 15 g per liters by connecting the reaction tank to an ultrafiltration unit equipped with 3000 MWCO regenerated cellulose cartridges. The concentrated depolymerized polysaccharide solution is diafiltered against 10 volumes of sterile physiological saline (0.85% sodium chloride). The depolymerized polysaccharide is stored at 1 to 5 deg. C. until the next process step. The molecular size of the depolymerized polysaccharide is determined by passage through a gel filtration chromatography column sold under the tradename "TJltahydrogel.TM.250" that is calibrated using Dextran molecular size standards and by multi-angle laser light scattering. The quantity of polysaccharide is determined by phospfcbrus content for serogroup A using the method of Bartlet, G. R. J. (1959) Journal of Biological Chemistry, 234, pp-466-468, and by the sialic acid content for serogroups C, W135 and Y using the method of Svennerholm, L. (1955) Biochimica Biophysica Acta 24, pp604-611. The 0-acetyl content is determined by the method of Hesterin, S. (1949) Journal of Biological Chemistry 180, p249. Reducing activity is determined by the method of Park, J. T. and Johnson, M. J. (1949 Journal of Biological Chemistry 181, ppl49-151. The structural integrity of the depolymerized polysaccharide is determined by protein .sup.lH and .sup.l3C NMR. The purity of the depolymerized polysaccharide is determined by measuring the LAL (endotoxin) content and the residual hydrogen peroxide content. 21 Example 3 Derivatization of Neisseria meningitidis Serogroups A, C, W-135, and Y Depolymerized Polysaccharide Materials used in this preparation include hydrogen peroxide depolymerized capsular polysaccharide serogroups A, C, W-135, and Y from Neisseria meningitidis (prepared in accordance with Example 2), adipic acid dihydrazide, l-ethyl-3-(3-dimethylaminopropyl) carbodiimide (EDAC) for serogroup A only, sodium cyanborohydride, sterile IN hydrocholoric acid, sterile IN sodium hydroxide, sterile 1 M sodium chloride, and sterile physiological saline (0.85% sodium chloride). Each serogroup polysaccharide is derivatized in a separate reaction. A stainless steel tank is charged with the purified depolymerized polysaccharide, and diluted with sterile 0.85% physiological saline to achieve a final reaction concentration of 6 g polysaccharide per liter. To this solution is added a concentrated aliquot of adipic acid dihydrazide dissolved in sterile 0.85% physiological saline, in order to achieve a reaction concentration of lg per liter. For serogroup A only, EDAC is added as a concentrated aliquot dissolved in sterile 0.85% physiological saline, to achieve a reaction concentration of lg per liter. The pH is adjusted to 5.0.+-.0.1, and this pH is maintained for 2 hours using sterile IN hydrochloric acid and sterile IN sodium hydroxide at room temperature (15 to 30 deg. C). After two hours, a concentrated aliquot of sodium cyanoborohydride, dissolved in 0.85% physiological saline, is added to the reaction mixture to achieve a reaction concentration of 2 g per liter. The reaction is stirred at room temperature (15 to 30 deg. C.) for 44 hours.+-.4 hours while maintaining the pH at 5.5.+-.0.5. Following this reaction period, the pH is adjusted to 6.0.+-.0.1, and the derivatized polysaccharide is concentrated to 12 g polysaccharide per liter by connecting the reaction tank to a ultrafiltration unit equipped with a 3000 MWCO regenerated cellulose cartridges. The concentrated, derivatized polysaccharide is diafiltered against 30 volumes of 1 M sodium chloride, followed by 10 volumes of 0.15 M sodium chloride. The tank is disconnected from the ultrafiltration unit and stored at 1 to 5 deg. C. for 7 days. The tank is reconnected to an ultrafiltration unit equipped with 3000 MWCO regenerated cellulose cartridges, and diafiltered against 30 volumes of 1 M sodium chloride, followed by 10 volumes of 0.15 M sodium chloride. 22 The molecular size of the derivatized polysaccharide, the quantity of polysaccharide, and the O-acetyl content are measured by the same methods used on the depolymerized polysaccharide. The hydrazide content is measured by the 2,4,6-trinitrobenzensulfonic acid method of Snyder, S. L. and Sobocinski, P. Z. (1975) Analytical Biochemistry 64, pp282-288. The structural integrity of the derivatized polysaccharide is determined by proton 1H and 13C NMR. The purity of the derivatized polysaccharide is determined by measuring the level of unbound hydrazide, the LAL (endotoxin) content, and the residual cyanoborohydride content. Example 4 Preparation of Carrier Protein Preparation of Crude Diphtheria Toxoid Protein Lyophilized seed cultures are reconstituted and incubated for 16 to 18 hours. An aliquot from the culture is transferred to a 0.5-liter flask containing growth medium, and the culture flask is incubated at 34.5 to 36.5 deg. C. on a rotary shaker for 7 to 9 hours. An aliquot from the culture flask is transferred to a 4-liter flask containing growth medium, and the culture flask is incubated at 34.5 to 36.5 deg. C. on a rotary shaker for 14 to 22 hours. The cultures from the 4-liter flask are used to inoculate a fermenter containing growth media. The fermenter is incubated at 34.5 to 36.5 deg. C. for 70 to 144 hours. The contents of the fermenter are filtered through depth filters into a collection vessel. An aliquot of formaldehyde solution, 37% is added to the harvest to achieve a concentration of 0.2%. The pH is adjusted to 7.4 to 7.6. The harvest is filtered through a 0.2 micron filter cartridge into sterile 201iter bottles. The bottles are incubated at 34.5 to 36.5 deg. C. for 7 days. An aliquot of formaldehyde solution, 37%, is added to each 201iter bottle to achieve a concentration of 0.4%. The pH of the mixtures is adjusted to 7.4 to 7.6. The bottles are incubated at 34.5 to 36.5 deg. C. for 7 days on a shaker. An aliquot of formaldehyde solution, 37%, is added to each 20 liter bottle to achieve a concentration of 0.5%. The pH of the mixtures is adjusted to 7.4 to 7.6. The bottles are incubated at 34.5 to 36.5 deg. C. for 8 weeks. The crude toxoid is tested for detoxification. The bottles are stored at 1 to 5 deg. C. during the testing period. Purification of the Crude Diphtheria Toxoid Protein The crude toxoid is allowed to warm to room temperature, and the contents of the 20-liter 23 bottles are combined into a purification tank. The pH of the toxoid is adjusted to 7.2 to 7.4, and charcoal is added to the crude toxoid and mixed for 2 minutes. The charcoal toxoid mixture is allowed to stand for 1 hours, and is then filtered through a depth filter cartridge into a second purification tank. Solid ammonium sulfate is added to the filtrate to achieve 70% of saturation. The pH is adjusted to 6.8 to 7.2, and the solution is allowed to stand for 16 hours. The precipitated protein is collected by filtration and washed with 70% of saturation ammonium sulfate solution, pH 7.0. The precipitate is dissolved into sterile distilled water, and the protein solution is filtered into a stainless steel collection vessel. The pH is adjusted to 6.8 to 7.2, and ammonium sulfate is added to 40% of saturation. The pH of the solution is adjusted to 7.0 to 7.2, and the solution is allowed to stand for 16 hours. The precipitate is removed by filtration and discarded. Ammonium sulfate is added to the filtrate to 60% of saturation, and the pH adjusted to 7.0 to 7.2. The mixture is allowed to stand for 16 hours, and the precipitated protein is collected by filtration. The precipitate is dissolved into sterile distilled water, filtered to remove undissolved protein, and diafiltered against 0.85% physiological saline. Concentration and Sterile Filtration of the Purified Diphtheria Toxoid Protein The protein solution is concentrated to 15 g per liter and diafiltered against 10 volumes of 0.85% physiological saline suing a 10,000 MWCO regenerated cellulose filter cartridge. The concentrated protein solution is sterilized by filtration through a 0.2 micron membrane. The protein solution is stored at 1 to 5 deg. C. until processed onto conjugate. The protein concentration is determined by the method of Lowry, O. H. et. al (1951) Journal of Biological Chemistry 193, p265-275. The purity of the protein is measured by sterility, 25 LAL (endotoxin) content, and residual formaldehyde content. Example 5 Preparation of Monovalent Conjugates of Neisseria meningitidis Serogroups A, C, W-135, and Y Polysaccharide to Diphtheria Toxoid Protein Materials used in this preparation include adipic acid derivatized polysaccharide from Neisseria meningitidis serogroups A, C, W-135, and Y (prepared in accordance with Example 3), sterile diphtheria toxoid protein (prepared in accordance with Example 4), EDAC, ammonium sulfate, sterile IN hydrochloric acid, sterile IN sodium hydroxide, and 24 sterile physiological saline (0.85%). Each serogroup polysaccharide conjugate is prepared by a separate reaction. All four conjugates are prepared by the following process. A stainless steel tank is charged with the purified adipic acid derivatized polysaccharide at a reaction concentration of 700 to 1000 .mu.moles of reactive hydride per liter and purified diphtheria toxoid protein at a reaction concentration of 3.8 to 4.0 g protein per liter. Physiological saline 0.85%, is used to dilute the starting materials to the target reaction concentrations and the pH is adjusted to 5.0.+-.0.1. An aliquot of EDAC is added to the polysaccharide protein mixture to achieve a reaction concentration of 2.28 to 2.4 g per liter. The pH of the reaction is kept at 5.0.+-.0.1 for 2 hours at 15 to 30 deg. C. After two hours, the pH is adjusted to 7.0.+-.0.1 using sterile IN sodium hydroxide, and the reaction is stored at 1 to 5 deg. C. for 16 to 20 hours. The reaction mixture is allowed to warm to 15 to 30 deg. C. and the reaction vessel is connected to an ultrafiltration unit equipped with a 30,000 MWCO regenerated cellulose cartridge. Solid ammonium sulfate is added to 60% of saturation .(for serogroups A, W-135 and Y) and 50% of saturation (for serogroup C). The conjugate reaction mixture is diafiltered against 20 volumes of 60% of saturated ammonium sulfate solution (for serogroups A, W-135 and Y) and 50% of saturated ammonium sulfate solution (for serogroup C), followed by 20 volumes of physiological saline, 0.85%. The diafiltered conjugate is first filtered through a filter capsule containing a 1.2 micron and a 0.45 micron filter, and then through a second filter capsule containing a 0.22 micron filter. The quantity of polysaccharide and O-acetyl content are measured by the same methods used on the depolymerized and derivatized polysaccharide. The quantity of protein is determined by the Lowry method. The molecular size of the conjugate is determined by passage through a gel filtration chromatography column sold under the tradename "TSK6000PW" that used DNA as the void volume marker, ATP as the total volume marker, and bovine thyroglobulin as a reference marker. In addition, the molecular size of the conjugate eluted from the TKS6000PW column is measured by multi-angle laser light scattering. The antigenic character of the conjugate is measured by binding to anti-polysaccharide serogroup specific antibody using double-sandwich ELISA method. The purity of the conjugates is determined by measuring the amount of unbound (unconjugated) polysaccharide by elution though a hydrophobic interaction chromatography column, 25 unconjugated protein by capillary electrophoresis, sterility, LAL (endotoxin) content, residual EDAC content, and residual ammonium ion content. Example 6 Formulation of a Multivalent Meningococcal A, C, W-135, and Y 5 Polysaccharide Diphtheria Toxoid Conjugate Vaccine Materials used in this preparation include, serogroups A, C, W-135, and Y polysaccharide-diphtheria toxoid conjugates that are prepared in accordance with Example 5, sterile 100 mM sodium phosphate buffered physiological saline (0.85% sodium chloride). An aliquot of sterile 100-500 mM sodium phosphate buffered physiological saline is added to physiological saline (0.85%) in a stainless steel bulking tank to yield a final vaccine concentration of 10 mM sodium phosphate. An aliquot of each of from two to four of the sterile monovalent meningococcal polysaccharide-diphtheria toxoid conjugates is added to the bulking tank containing 10 mM sterile sodium phosphate physiological saline to yield a final concentration of 8 jig of each serogroup polysaccharide per milliliter of buffer. The formulated tetravalent conjugate is mixed and filtered through a 0.2 .mu.m filter into a second bulking tank. The quantity of each serogroup polysaccharide present in the multivalent formulation is determined by component saccharide analysis using high pH anion-exchange chromatography with pulsed amperometric detection. The quantity of protein is measured by the method of Lowry. Th pH of the vaccine is measured using a combination electrode connected to a pH meter. The antigenic character of the multivalent conjugate vaccine is measured by binding to anti-polysaccharide serogroup specific antibody using a double-sandwich ELISA method. Immunogenicity of the multivalent conjugate vaccine is measured the ability of each conjugate present in the vaccine to elicit both a primary and booster anti-polysaccharide IgG immune response in an animal model. The purity of the multivalent conjugate vaccine is determined by measuring the amount of unbound (unconjugated) polysaccharide using high pH anion-exchange chromatography with pulsed amperometric detection, sterility, LAL (endotoxin) content, pyrogenic content, and general safety. 26 Example 7 Preparation of Aluminum-hydroxide Adjuvanted Multivalent Meningococcal Polysaccharide Diphtheria Toxoid Protein Conjugate Preparation of conjugate adsorbed to aluminum hydroxide. Materials used in this preparation include serogroups A, C, W-135, and Y polysaccharifie-diphtheria toxoid conjugates that are prepared in accordance with Example 5, sterile physiological saline (0.85% sodium chloride), and sterile aluminum hydroxide in physiological saline (0.85% sodium chloride). An aliquot of each of the sterile monovalent meningococcal polysaccharide diphtheria toxoid conjugates is added to the bulking tank containing physiological saline to yield a final concentration of 8 ug of each serogroup polysaccharide per milliliter of buffer. An aliquot of sterile aluminum hydroxide in physiological saline (0.85% sodium chloride) is added to the multivalent conjugate vaccine to achieve a final concentration of 0.44 mg aluminum ion per milliliter vaccine. Example 8 Preparation of Aluminum Phosphate-adjuvanted Conjugate Materials used in this preparation include serogroups A, C, W-135, and Y polysaccharide-diphtheria toxoid conjugates that are prepared according to Example 5, sterile physiological saline (0.85% sodium chloride), and sterile aluminum phosphate in physiological saline (0.85% sodium chloride). An aliquot of each of the sterile monovalent meningococcal polysaccharide-diphtheria toxoid conjugates is added to the bulking tank containing physiological saline to yield a final concentration of 8 ug of each serogroup polysaccharide per milliliter of buffer. An aliquot of sterile aluminum phosphate in physiological saline (0.85% sodium chloride) is added to the multivalent conjugate vaccine to achieve a final concentration of 0.44 mg aluminum ion per milliliter vaccine. 27 Example 9 General Description of Materials and Methods Used in Human Clinical Studies Immunogenicity of a Tetravalent Derivatized Conjugate Vaccine The conjugate vaccine is studied for its ability to elicit an immune response in humans under a number of different clinical protocols. The following studies summarize the results. The materials and methods used in each of the following studies, unless indicated otherwise, are: TetraMenD TetraMenD vaccine comprises four meningococcal capsular polysaccharides of serogroups A, C, Y, and W-135,4 ug of each polysaccharide, covalently attached to a total of 48 ug diphtheria toxoid protein. The vaccine is. formulated in sterile, pyrogen-free, phosphate-buffered physiological saline, with no preservative. The formula comprises 0.6 mg sodium phosphate, 4.4 mg sodium chloride and up to 0.5 rnL water. Menomune® Menomune® is licensed in the United States and elsewhere for use .among persons aged 2 years and older. Menomune is a freeze-dried preparation, each dose of vaccine containing 50 ug of each A, C, Y and W-135 polysaccharide as antigens, reconstituted with a diluent of isotonic sodium chloride solution preserved with thimerosal and given subcutaneously as a 0.5 mL dose. Each 0.5 mL dose of vaccine contains 2.5 mg to 5 mg of lactose as a stabilizer. Menomune®- A/CA7W-135, Meningococcal Polysaccharide Vaccine, Groups A, C, Y, and W-135 Combined, for subcutaneous use, is a freeze-dried preparation of the group-specific polysaccharide antigens from Neisseria meningitidis, Group A, Group C, Group Y, and Group W-135. The diluent is sterile, pyrogen-free, distilled water. After reconstitution of the lyophilized product with diluent as indicated on the label, each 0.5 mL dose is formulated to contain 50 ug of "isolated product" from each of the serogroups A, C, Y, and W-135 in isotonic sodium chloride solution. Tetanus and Diphtheria Toxoids Adsorbed for Adult Use® (referred to subsequently as Td) is a sterile suspension of alum precipitated toxoid in an isotonic sodium chloride solution containing sodium phosphate buffer to control pH. The vaccine is for intramuscular injection. Each 0.5mL dose is formulated to contain 5Lf of tetanus toxoid, 2Lf of diphtheria 28 toxoid and not more than 0.28 mg of aluminum by assay. Tetanus and diphtheriatoxoids induce at least 2 units and 0.5 units of antitoxin per mL respectively in the guinea pig potency test. At visit 1, Td is administered to all participants as a single 0.5mL dose by intramuscular injection using a one inch 25 gauge needle into the deltoid of the left arm. Each 0.5mL dose contains 5Lf of tetanus toxoid and 2Lf of diphtheria toxoid. Sera Samples Blood specimens are drawn on the Days indicated after the baseline. For example, if the protocol indicates three time points, DO, D28 and 6 Month, then blood specimens are drawn on Day 0 prior to vaccination (baseline), at Day 28 post-vaccination (to assess primary immune response, and at 6 month post-vaccination (to assess the longevity of the immune response). Approximately 5 mL of whole blood is collected from each subject at each time point. The whole blood is centrifuged within four hours of collection. The serum is removed and stored at -20 deg. C. A "Day 28" blood sample is taken at least 28 days but not yet 57 days after the Day 0 injection. A "6 month" blood sample is taken at 6 months plus or minus 28 days after the Day 0 injection. Thus, a Day 28 sera represents a sera is drawn between day 28 to day 56 after DO; and a 6 month sera represents a sera is drawn between day 149 to day 217 after DO. Assay Techniques The present studies utilize a number of standard immunological assays. The following descriptions summarize the methodologies used herein. However, other similar assays, including variations of those presented herein, are well known by those in the art and may be utilized. Anti-Meningococcal Antibody Determination by a Serum Bactericidal Assay using Baby Rabbit Complement (SBA-BR) Functional antibody activity for anti-meningococcal antibody to serogroups A, C, Y, and W-135 is measured using a serum bactericidal assay. Two-fold dilutions of test sera are prepared in sterile 96-well microtiter plates. Serogroup specific meningococcal bacteria along with baby rabbit complement are added to the serum dilutions and allowed to incubate. After this incubation period, an agar overlay medium is added to the serum/complement/bacteria mixture, allowed to harden, and then incubated overnight at 29 37°C with 5% C02. Bacterial colonies present in the wells are counted. The endpoint titer is determined by the reciprocal serum dilution yielding > 50% killing as compared to the mean of the complement control wells. The limit of detection for this assay, using rabbit complement, is a titer of S. IgG Anti-Meningococcal Antibody Determination IgG antibody activity for anti-meningococcal antibody to serogroups A, C, Y, and W-135 is measured using an indirect ELISA. This procedure involves reacting antibody in sera with excess meningococcal group specific polysaccharide (MenPs) antigen adsorbed to plastic microtiter wells by methylated human serum albumin. The amount of bound antibody is determined by a reaction with peroxidase-labeled mouse anti-human IgG specific monoclonal antibody. A subsequent reaction using peroxidase substrate generates a chromogenic product that is measured spectrophotometrically. The resulting optical density (OD) correlates with the amount of IgG antibody in the serum that is bound to the meningococcal polysaccharide on the microtiter plate. The amount of IgG antibody is then calculated by comparison to a reference (Lot CDC 1992 or equivalent) with an assigned value using a 4-parameter logistic curve method. IgM Anti-Meningococcal Antibody Determination IgM antibody activity for anti-meningococcal antibody to serogroups A, C, Y, and W-135 is measured using an indirect ELISA. This procedure involves reacting antibody in sera with excess MenPs antigen adsorbed to plastic microtiter wells by methylated human serum albumin. The amount of bound antibody is determined by a reaction with peroxidaselabeled mouse anti-human IgM specific monoclonal antibody. A subsequent reaction using peroxidase substrate generates a chromogenic product that is measured spectrophotometrically. The resulting OD correlates with the amount of IgM antibody in the serum that is bound to the meningococcal polysaccharide on the microtiter plate. The amount of IgM antibody is then calculated by comparison to a reference (Lot CDC 1992 or equivalent) with an assigned value using a 4-parameter logistic curve. High Avidity Anti-Meningococcal IgG Antibody Determination High avidity IgG antibody activity for anti-meningococcal antibody to serogroups A, C, Y, and W-135 will be measured at Aventis Pasteur Inc. using a modified ELISA. This assay is 30 currently under development at Aventis Pasteur Inc. and will be qualified prior to testing of clinical specimens. Briefly, 96 well microtiter plates are coated with MenPs antigen. After aspirating and ishing the coated plates, serial dilutions of clinical sera are prepared directly in the plates, using phosphate buffered saline (PBS) serum diluting buffer containing 75 mM ammonium thiocyanate, and allowed to incubate overnight. The amount of bound antibody is determined by a reaction with peroxidase-labeled mouse anti-human IgG specific monoclonal antibody. A subsequent reaction using peroxidase substrate generates a chromogenic product that is measured spectrophotometrically. The resulting OD correlates with the amount of high avidity IgG antibody in the serum that is bound to the meningococcal polysaccharide on the microtiter plate. The amount of high avidity IgG antibody is then calculated by comparison to a reference (Lot CDC 1992 or equivalent) using a 4-parameter logistic curve. IgGl and IgG2 Subclass Meningococcal Antibody Determination IgGl and IgG2 subclass antibody distribution for anti-meningococcal antibody to serogroups A, C, Y and W-135 is measured using an ELISA. Antibody present in serial dilutions of sera is reacted with MenPs antigen adsorbed to the wells of microliter plates. The amount of bound antibody will be determined using anti-human IgGl Fc or IgG2 Fc specific reagents. A subsequent reaction with enzyme substrate generates a chrombgenic product that is measured spectrophotometrically. The resulting OD correlates with the amount of IgGl or IgG2 antibody in the serum that is bound to the meningococcal polysaccharide on the microtiter plate. The amount of antibody will be reported as the IgGl :IgG2 ratio in the serum specimen or as the concentration of IgGl or IgG2 in the specimen if a suitable reference is available. Anti-Diphtheria Antibody Determination By Metabolic Inhibition of VERO Cells Anti-diphtheria antibody responses are measured by the ability of the test sera to protect VERO cells from a diphtheria toxin challenge. Using sterile 96-well microtiter plates, two-fold dilutions of test sera, beginning with a 1:4 dilution, are challenged with diphtheria toxin and allowed to incubate. VERO cells are then added, the wells sealed with sterile mineral oil and incubated for six to eight days. Antibody levels are then determined by observing a color change of the pH indicator in the media resulting from the byproducts of cell metabolism. Results are reported as International Units/mL by comparison to a calibrated 31 WHO reference serum and determined by the highest serum dilution that allows cell metabolism in the presence of the challenge dose of diphtheria toxin. The lower limit of detection is determined by the minimum detectable antitoxin level of the reference serum, and the starting dilution of the test sera, and is typically 0.005 IU/mL. Anti-Tetanus Antibody Determination By Elisa Anti-Tetanus antibody levels are determined by an indirect Enzyme Linked Immunosorbent Assay (ELISA). The method involves reacting antibody in test sera with tetanus toxoid adsorbed to plastic microtiter wells. The amount of bound antibody is determined by a reaction with Goat Anti-Human IgG-specific antibody conjugated to alkaline phosphatase. A subsequent reaction with alkaline phosphatase substrate generates a chromogenic"product that is measured spectrophotometrically. The OD (optical density) correlates with the amount of antibody in the serum dilution that binds to the antigen coated microtiter plate. The antibody concentration is calculated by comparison to an international human reference (WHO Lot TE-3) with assigned linkage by a Parallel Line Analysis method. Results are reported as International Units per milliliter (IU/mL). The minimum level of quantitation for the anti-tetanus IgG ELISA is 0.01 IU/mL, with samples resulting in values lower than this level reported as As used herein, "Adverse Event", "Serious Adverse Experience", and "Unexpected Adverse Experience" are terms well understood within the vaccine industry. The safety data are summarized and analyzed in accordance with standard clinical practice, which including assessing all participants who received vaccine for the duration of the clinical study. In general, each of the terms is understood to have the following meanings. Adverse Event (AE) is defined as "any untoward medical occurrence in a patient or clinical investigation subject administered a pharmaceutical product and that does not necessarily have a causal relationship with this treatment. An adverse event can therefore be any unfavorable and unintended sign (including an abnormal laboratory finding), symptom, or disease temporally associated with the use of a medicinal (investigational) product, whether or not related to the medicinal (investigational) product." (ICH guidelines, GCP (E6) § 1.2). 32 Serious Adverse Experience (SAE) is "any adverse drug experience occurring at any dose that results in any of the following outcomes: death, a life-threatening adverse drug experience, inpatient hospitalization or prolongation of existing hospitalization, a persistent or significant disability/incapacity, or a congenital anomaly/birth defect. Important medical events that may not result in death, be life-threatening, or require hospitalization may be considered a serious adverse drug experience when, based upon appropriate medical judgment, they may jeopardize the patient or subject and may require medical or surgical intervention to prevent one of the outcomes listed in this definition. Examples of such medical events include allergic broncho spasm requiring intensive treatment in an emergency room or at home, blood dyscrasias or convulsions that do not result in inpatient hospitalization, or the development of drug dependency or drug abuse." (21 CFR Ch. I, §312.32(a)). Unexpected Adverse Experience (UAE) is "any adverse drug experience, the specificity or severity of which is not consistent with the current investigator"s brochure; or, if an investigator brochure is not required or available, the specificity or severity of which is not consistent with the risk information described in the general investigational plan or elsewhere in the current application, as amended." (21 CFR Ch. I, §312.32(a)). The studies conducted in accordance with standard clinical practice, and the criteria for 20 enrollment or exclusion of patients in the studies are: Inclusion criteria for patients: 1. Participant is healthy, as determined by medical history and physical examination. 2. Participant is at least 11 years of age but not yet 19 years of age at the time of vaccination. 3. Parent/guardian or participant has signed Institutional Review Board (IRB) approved informed consent form where applicable. 4. Participant has signed Institutional Review Board (IRB) approved assent form where applicable Exclusion criteria for patients: 30 33 I. Serious chronic disease (i.e. cardiac, renal, neurologic, metabolic, rheumatologic, etc.). 2. Known or suspected impairment of immunologic function. 3. Acute medical illness with or without fever within the last 72 hours or an oral 5 temperature 38°C (100.4°F) at the time of inclusion. 4. History of documented invasive meningococcal disease or previous meningococcal vaccination. 5. Administration of immune globulin, other blood products within the last 3 months, or oral or injected corticosteroids or other immunomodulatory therapy within 6 weeks of the study vaccine. Individuals on a tapering dose schedule of oral steroids lasting 6. Antibiotic therapy within the 72 hours prior to vaccination 7. Received any vaccine in the 28-day period prior to enrollment, or scheduled to 15 receive any vaccination in the 28-day period after enrollment, except where the study notes additional vaccinations. 8. Suspected or known hypersensitivity to any of the vaccine components. 9. Unavailable for the entire study period or unable to attend the scheduled visits or to comply with the study procedures. 10. Enrolled in another clinical trial. II. Any condition which, in the opinion of the investigator, would pose a health risk to . ; lit the participant or interfere with the evaluation of the vaccine. 12. In females, a positive or equivocal urine pregnancy test at the time of vaccination. Example 10 Study A -Dosage Study Study A is an unblinded, open-label, dose-escalation trial of three dosage levels of TetraMenD vaccine, administered to participants in three age groups. Ninety healthy adults (18 to 55 years of age) are enrolled in Stage I and received a single injection of TetraMenD vaccine. Thirty healthy children (12 to 22 months of age) are enrolled in Stage II and received 2 injections of a single dosage level of TetraMenD vaccine. Ninety healthy infants 34 (6 to 12 weeks of age) are enrolled in Stage in and received 3 injections of a single dosage level of TetraMenD vaccine. Stage IDosage Study in Adults 18 to 55 Years This clinical trial is an unblended, open-label, dose-escalation trial of three dosage levels of TetraMenD vaccine, which is administered to participants in three age groups. In Stage 1, ninety healthy adults (18 to 55 years of age) receive a single injection of TetraMenD vaccine. For adult participants, serum specimens for serologic analysis are obtained at baseline (day 0) prior to TetraMenD administration, and at day 28 after TetraMenD administration. All available specimens are analyzed for SBA against meningococcal polysaccharide serogroups A, C, Y, and W-135, and by ELISA for IgG antibody against these same serogroups. The SBA and IgG ELISA findings for all serogroups are summarized below. One key immunogenicity endpoint is the proportion of participants with a >_4-fold rise from baseline. To determine what effect the baseline SBA titer had on the proportion with a >_4-fold rise in SBA, a subgroup analysis is performed for adults whose baseline titer for each particular antigen is less than 1:64, and adults whose baseline titer for that particular antigen is at least 1:64. The safety profile of TetraMenD is comparable to that of Menomune®. The results of this Study are summarized in the following Tables. 35 Table A-1:Serogroup & dosaee level NDo stage I (An ND0 SBA (A) 1 μg 26 l (3.8) l (3.8) - i(3.8) " 4 (15.4) — 9 (34.6) 4μg 28 2 (7.1) - - 1 (3.6) 3 (10.7) 1 (3.6) 2 (7.1) 3 (10.7) 10μg 27 1 (3.7) ■ 1 2 (3.7) (7.4) 2 (7.4) 2(7.4) 6 (22.2) SBA (C) L μg 26 15 (57.7) " ~ 1 1 (3.8X3.8) 6 (23.1) ~ 1 (3.8) 4 μg 28 18 (64.3) 1 (3.6) 1 (3.6) 3 (10.7) 2(7.1) L0μg 27 17 (63.0) - 1 (3.7) ~ ~ 2 (7.4) 2(7.4) 3 (11.1) SBA (Y) 1μg 26 15 (57.7) 1 (3.8) 4 (15.4) 2(7.7) 3 (11.5) 1 (3.8) " ~ 4μg 28 15 (53.6) - 4(14.3 3 10.7) 3 (10.7); 1 (3.6) 1 (3.6) 10 μg 27 10 (37.0) 1 (3.7) 2(7.4) 2(7.4) 6 (22.2) 2(7.4) 2(7.4) - SBA(W-135) ...ii> 1μg 26 18 (69.2) 1 (3.8) ~ 1 (3.8) 1 (3.8) - 1 (3.8) 1 (3.8) 4μg 28 13 (46.4) 8 (28.6) 2(7.1) 1 (3.6) 1 (3.6) 1 (3.6) 1 (3.6) 1 (3.6) 10μg 27 19 (70.4] 1 (3.7) 2(7.4) " 1 (3.7) 1 (3.7) 1 (3.7) (3.7) 36 Serogroup & NDf Table A-1: Stage(Adults)- Distribution of SBA Titers at Baseline May 0) by TetraMenD Dosage Level n* (%) of Participants with Titer Result8 1024 to 65536 dosage level 1024 2048 4096 8192 16384 32768 65536 SBA (A) 1 μg 26 2 (7.7) 6 (23.1) 1(3.8) 1(3.8) ~ ~ " 4μg 28 5 (17.9) 10 35.7) 1 (3.6) - _ • 10 μg 27 5 (18.5) 6 (22.2) 2(7.4) . ■ "■t . - SBA (C) 1μg 26 - 2(7.7) - - - ■ - - 4μg 28 3 (10.7) - - - : - - 10μg 27 2 (7.4) - - - - - - SBA (Y) Iμg 26 - - - - - - - 4μg 28 - - - 1 (3.6) - - - - lOμg 27 - 1 (3.7) 1 (3.7) - - - SBA (W-135) 1 μg 26 2(7.7) 1 (3.8) - - ■"-" - - 4μg 28 - - - - - _ 10 μg 27 1 (3.7) - - - ■ - - 37 Serogroup & dosaee level Table A-2: Stage I(Adults) - Distribution of SBA Titers at Day 28 Post-. Injection, by MenD Dosage Level (Per-Protocol Population) n* (%) of Participants with Titer Result" SBA (A) 1μg 26 - - - - - 1 3.8) 1 (3.8) 2(7.7) 4μg 28 - - - - - - - - 10 μg 27 - - - - - - - - SBA (C) 1μg 26 3 (11.5) ™ *" ■ " 4 (15.4) 5 (19.2) 4μg 28 - 1 (3.6) - - 2 (7.1) - 1 |(3.6) 1 (3.6) 10μg 27 - 1 (3.7) " 2(7 4) 1 (3.7) 4 (14.8) SBA(Y) 1μg 26 4(15 4 ) 13 8 - 415 4 519 2 4 154 13 8 277 4μg 28 310 7 1(3 6 ) - 4(14 3) 1(36) 1(36) ■ 3(107) 10 μg 27 3(11 1) - 2(74) 5 (l8.5) 1 (3.7) 4 (14.8) SBA(W-135) 1 μg 26 (11.5) (7.7) (3.8) (3.8) (15.4) 4μg 28 4(14 3) - - 1(3 6) 2(7 1) 3(10 7 ) 10μg 27 - - - 2(7.4)\ 2 . ((7.4)\ 2(7.4) 38 Table A-3: Stage I (Adults) - Proportions Achieving SBA Thresholds at Baseline and at Day 28 Post-Injection, By TetraMenD Dosage Level (Per-Protocol Population) 39 Sero-group &d level NDO/N D28 % Achieving Threshold > • :8 > 1 :16 > 1 :32 > 1 :64 Day 0 D 8 Day 0 D 8 Day 0 Day 2 8 Day 0 2Day 8 SBA (A) 1 μg 26/26 96.2 100.0 92.3 100.0 92.3 100.0 88.5 100.0 4 μg 28/28 92.9 100.0 92.9 100.0 92.9 100.0 89.3 100.0 10 μg 27/27 100.0 100.0 96.3 100.0 96.3 100.0 92.6 100.0 SBA. (C) 1 μ9 26/26 42.3 88.5 42.3 88.5 42.3,,., 88.5 38.5 88.5 4 μg 28/28 35.7 100.0 32.1 96.4 32.1 96.4 28.6 96.4 10 μg 27/27 37.0 100.0 37.0 100.0 33.3 96.3 33.3 96.3 SBA (Y) 1 μg 26/26 42.3 84.6 38.5 80.8 23.1 80.8 15.4 65.4 4 μg 28/28 46.4 89.3 46.4 85.7 46.4 85.7 32.1 71.4 10 Pig 27/27 63.0 88.9 59.3 88.9 51.9 88.9 44.4 81.5 SBA (W-135) 1 Pig 26/26 30.8 88.5 26.9 88.5 26.9 88.5 23.1 80.8 4 pig 28/28 " 53.6 85.7 25.0 85.7 17.9 85.7 14.3 85.7 10 pig 27/27 29.6 100.0 25.9 100.0 18.5 100.0 18.5 100.0 N: number of evaluable participants at each time point (day 0; day 28) 40 Table A-4: Stage I (Adults) - SBA and IgG ELISA Results at Baseline and at Day 28 Post-Injection , by TeraMenD Dossage Level ( Per-Protocal Population ) Serogroup & dosage level NDO/ND2 8 GMT/GMC*(95% CI ) Mean Fold 1at Day 28 (95% CI) % >_4-Fold DayO Day 28 SBA (A) lμg 26/26 460.2 (223.0-949.7) 3054.9 (1872.9-4982.9) 6.6(2.9-15.4) 65.4 4μg 28/28 487.3 (231.2-1027.2) 6720.2 (4666.5-9677.7) 13.8 "" (6.0-31.7) 71.4 10 pig 27/27 525.3 (286.6-962.9) 10865.1 (7651.5-15428.2) 20.7 (11.7-36.6) 96.3 SBA(C) lμg 26/26 20.9 (8.8-49.6) 540.0 (238.1-1224.7) 25.9 (9.7-68.6) 73.1 4μg 28/28 16.4 (7.1-37.7) 1559.8 (799.9-3041.5) " 95.1 (39.7-227.7) 89.3 10 μg 27/27 19.2 (8.0-45.8) 1755.6 (880.5-3500.4) 91.7 (37.6-223.5) 96.3 SBA(Y) lμg 26/26 9.4 (5.9- 4.9) 95.5 (40.5-225.0) 10.2 (4.9-20.9) 73.1 4μg 28/28 19.0 (8.8-41.2) 390.0 (143.3-1061.3) , 20.5 (8.9-47.4) 82.1 10 μg 27/27 28.1 (12.9-61.6) 386.0 (145.2-1026.2) 13.7 (5.8-32.7) 66.7 SBA (W-135) lμg 26/26 13.6 (5.7-32.4) 498.5 (203.2-1223.2) 36.6 (13.7-97.7) 76.9 4μg 28/28 10.0 (5.9-16.9) 608.9 (250.3-1480.9) 60.9 ,(23.7-156.7) 85.7 10 μg 27/27 9.8 (5.0-19.1) 1848.1 (1075.4-3176.2) 188.1 (94.0-376.7) 100.0 IgG ELISA (A) lμg 26/26 3.4 (1.8-6.6) 19.4 (11.6-32.3) 5:7. (3.8-8.3) 69.2 4μg 28/28 3.3 (2.3-4.8) 38.4 (22.2-66.4) 11.5 (7.4-18.0) 75.0 10 μg 27/27 3.1 (1.7-5.6) 56.4 (31.8-99.9) 18.1 (12.2-26.9) 88.9 41 Table A-4: Stage I (Adults) - SBA and IgG ELISA Results at Baseline and at Day 28 Post-Injection, by TetraMenD Dosage Level (Per-Protocol Population) Serogroup & dosage level NDO/Nda 88 GMT/GMC* (95% CI) Mean Fold Tat Day 28 (95%CI) %>_4-Fold DayO Day 28 IgG ELISA( c) (Q 1μg 26/26 0.3 (0.2-0.5) 2.2 (1.2-4.1) 7.3 (4.0-13.4) 61.5 4μg 28/28 0.4 (0.2-0.7) 5.5 (3.0-10.1) 14.2(8.7-23.2) 82.1 10 μg 27/27 0.5 (0.3-0.9) 11.1 (5.5-22.5) 22.8 (13.4-38.8) 88.9 IgG ELISA (Y) Lμg 26/26 0.6 (0.4-1.0) 2.8 (1.5-5.2) 4.6 (2.7-7.6) 53.8 4μg 28/28 1.3 (0.7-2.5) 6.8 (3.2-14.6) 5.4 C3.2-9.05 53.6 10 μg 27/27 1.0 (0.5-2.1) 7.7 (3.4-17.2) 7.4 (5.1-10.8) 77.8 IgG ELISA (W- (135) lμg 26/26 0.5 (0.3-0.9) 2.3 (1.0-5.3) 4.4 (2.4^7.9) 46.2 4μg 28/28 0.6 (0.3-1.0) 5.8 (2.9-11.7) 10.2 (6.1-16.9) 71.4 10 μg 27/27 0.4 (0.2-0.7) 9.3 (4.8-18.1) 22.7 (11.9-43.2) 85.2 Day 0: Baseline blood sample drawn prior to vaccination. Day 28: Blood sample drawn 28 days following vaccination. % 4-fold rise: the percent of adults who had a 4-fold rise in GMT at day 28 in comparison to day O. N: number of evaluable participants *GMTs are computed for the SBA data; GMCs are computed for the IgG ELISA data. Table A-5 presents the GMT by dose, patient age and serogroup. Table A-5 GMT by Dose, patient age and Serogroup Age Dose TetraMenD No. of Subjects Blood Day A GMT CGMT WGMT YGMT 19 lμg 2 0 1024.00 512.00 45.25 8.00 1μg 2 28 2896.31 2048.00 2048.00 362.04 4|μg 2 0 2048.00 64.00 16.00 181.02 4|μg 1 2 28 8192.00 8192.00 , , 2048.00 2048.00 10 μg 10 0 1097.50 34.30 21.11 128.00 10μg 10 28 18820.27 3821.70 2352.53 1176.27 20 lμg 3 0 322.54 10.08 10.08 12.70 lμg 3 28 3251.00 203.19 2048.00 203.19 4μg 2 0 512.00 4.00 4.00 4.00 42 4μg 2 28 5792.62 128.00 22.63 22.63 10 μg 1 0 128.00 4.00 4.00 4.00 10 pig 1 28 16384.00 4096.00,." 128.00 2048.00 21 1μg 2 0 1024.00 22.63 32.00 256.00 1μg 1 28 8192.00 8192.00 2048.00 1024.00 4μg 3 0 812.75 12.70 4.00 256.00 t 4μg 3 28 10321.27 1024.00 5160.64 8192.00 22 " 1μg 2 0 1024.00 4.00 11.31 16.00 - 1 μg 2 28 4096.00 362.04 2048.00 512.00 4μg 2 3 128.00 45.25 5.66 16.00 4μg 2 28 8192.00 2896.31,,, 1024.00 2048.00 10 μg 2 3 2048.00 90.51 4.00 22.63 10 pig 2 28 16384.00 8192.00 512.00 512.00 23 1 μg 1 D 512.00 2048.00 2048.00 16.00 1μg 1 28 512.00 2048.00 2048.00 64.00 4μg 2 0 1448.15 4.00 4.00 45.25 4μg 2 28 4096.00 1448.15 1024.00 256.00 10μg 1 0 1024.00 128.00 4.00 64.00 10μg 1 28 16384.00 512.00 ... 8192.00 2048.00 24 4μg 2 0 181.02 11.31 90.51 4.00 4μg 2 28 11585.24 2896.31 1448.15 512.00 10 μg 1 0 1024.00 4.00 4.00 4.00 10 μg 1 28 16384.00 2048.00 4096.00 4.00 25 1μg 1 0 128.00 4.00 4.00 4.00 1μg 1 28 4096.00 4096.00 2048.00 32.00 10μg 2 0 1024.00 32.00 4.00 22.63 10 μg 2 28 8192.00 2896.31 1448.15 2048.00 26 1μg 2 0 2048.00 4.00 64.00 4.00 1 μg 2 28 4096.00 512.00 2896.31 1448.15 10 μg 2 0 362.04 45.25 22.63 4.00 10 μg 2 28 5792.62 2048.00 1448.15 32.00 27 1 μg 1 0 512.00 128.00 1024.00 4.00 1 μg 1 28 4096.00 1024.00 4096.00 4.00 4μg 2 0 90.51 22.63 64.00 16.00 4μg 2 28 16384.00 4096.00 1448.15 90.51 10 μg 1 0 512.00 4.00 128.00 64.00 10 μg 1 28 8192.00 16384.00 8192.00 16384.00 28 1μg 1 0 4.00 4.00 4.00 4.00 1μg 1 28 16384.00 1024.00 2048.00 256.00 4μg 2 0 724.08 64.00 8.00 11.31 4μg 2 28 5792.62 1448.15 2048.00 2048.00 10 μg 1 0 64.00 4.00 4.00 4.00 10 μg 1 28 4096.00 16.00 1024.00 4.00 30 4μg 1 0 32.00 4.00 16.00 32.00 4μg 1 28 16384.00 16384.00 8192.00 4096.00 31 1 μg 1 0 32.00 4.00 4.00 4.00 1 μg 1 28 8192.00 512.00 4.00 4.00 32 4μg 2 o 724.08 64.00 8.00 11.31 43 4μg ; 2 28 4096.00 1024.00 1148.15 128.00 33 1μg 2 3 2896.31 4.00 4.00 22.63 1 μg 2 28 2048.00 2048.00 724.08 512.00 4μg 1 3 1024.00 4.00 B.00 4.00 4μ9 1 28 32768.00 1024.00 4096.00 3192.00 34 4μg 1 0 64.00 128.00 ... 4.00 32.00 4μg 1 28 16384.00 8192.00 2048.00 512.00 35 1 μg : 2 3 724.08 16.00 5.66 32.00 1μg 2 28 2896.31 362.04 724.08 181.02 4μg 2I D 90.51 5.66 11.31 4.00 4μg 2 28 5792.62 5792.62 32.00 181.02 36 10μg 2 0 256.00 22.63 4.00 4.00 10 μg 2 28 11585.24 512.00 5792.62 256.00 37 1μg 1 0 4096.00 4.00 4.00 32.00 1μg 1 28 8192.00 2048.00 2048.00 64.00 10 μg 1 0 2048.00 4.00 8.00 4.00 10 μg 1 28 16384.00 2048.00 4096.00 64.00 39 1 μg 2 0 512.00 4.00 45.55 4.00 1μ9 2 28 5792.62 724.08 512.00 11.31 4μg 1 0 8192.00 4.00 8.00 4.00 4μ9 1 28 16384.00 2048.00 256.00 1024.00 40 1 μg 1 0 2048.00 4.00 ... , 4.00 4.00 1 μg 1 28 8192.00 4.00 128.00 64.00 41 1 μg 2 0 724.08 128.00 4.00 11.31 1μg 2 28 2896.31 362.04 128.00 128.00 42 4μg 2 0 362.04 45.25 22.63 128.00 4μg 2 28 2048.00 4096.00 2896.31 724.08 10 μg 1 0 128.00 4.00 4.00 8.00 10 μg 1 28 8192.00 2048.00 512.00 512.00 44 1μ9 1 0 B.00 32.00 4.00 4.00 1 μg 1 28 2048.00 512.00 4.00 8.00 4μg 1 0 512.00 4.00 16.00 4.00 4μ9 1 28 2048.00 512.00 2048.00 8.00 45 4μg 2 0 2048.00 4.00 5.66 4.00 4μ9 2 28 2896.31 128.00 4.00 16.00 10 μg 2 0 724.08 45.25 128.00 11.31 10 μg 2 28 2896.31 724.08 2896.31 181.02 46 1 μg 1 0 2048.00 128.00 4.00 4.00 1 μg 1 28 2048.00 256.00 4.00 4.00 47 10 μg 1 0 8.00 4.00 4.00 16.00 10 μ9 1 28 1024.00 128.00 512.00 4096.00 48 1 μg 1 0 128.00 512.00 4.00 16.00 1 μg 1 28 128.00 2048.00 512.00 128.00 49 10 μg 1 0 32.00 512.00 4.00 4.00 10 μg 1 28 8192.00 16384.0C ) 4096.00 64.00 52 10 μg 1 0 512.00 4.00 4.00 16.00 10 μg 1 28 32768.00 256.00 1024.00 32.00 54 1μg 1 o 512.00 4.00 4.00 16.00 44 lug 1 28 256.00 4.00 32.00 64.00 Stage II Dosage Study in Toddlers Aged 12 Months to 22 Months This clinical trial is an unblinded, open-label, dose-escalation trial of three dosage levels of TetraMenD vaccine, which is administered to participants in three age groups. In Stage II, thirty healthy children (12 to 22 months of age) receive two injections of a single dosage level of TetraMenD vaccine. For toddler participants, serum specimens for serologic analysis are obtained at three timepoints: at baseline (day 0) prior to TetraMenD injection #1, at day 60 after enrollment (60 days after injection #1 and immediately prior to TetraMenD injection #2), and at day 90 after enrollment (30 days after injection #2). All available specimens are analyzed for SBA against meningococcal polysaccharide serogroups A, C, Y, and W-135, and by ELISA for IgG antibody against these same serogroups. The SBA and IgG ELISA findings for all serogroups are summarized below. The results are summarized in the following Tables. 45 Table A-6: Stage H (Toddlers) - Distribution of SBA Titers at Baseline May 0) by TetraMenD Dosage Level (Per-Protocol Population) n* (%) of Participants with Titer Result* Serogroup & dosage level NDo SBA (A) lμg 4 (44.4) 2(22.2) - 1 (11.1) - 1 (11.1) 4μg 8 7 (87.5) - - - - - - 10pg 10 8 (80.0) ~ - 1 (10.0) - - ■ SBA (C) lμg 9 9 (100.0) - - - - - - 4pg 8 7 (87.5) - - - - ■» 1 (12.5) 10μg 10 7 (70.0) - 1 (10.0) - 2 20.0) ~ ~ SBA(Y) lμg 9 4 (44.4) 1 (11.1) 1 (11.1) 2(22.2) 1 (11.1) ■ ■ 4μg 8 5 (62.5) 2 (25.0) 1 (12.5) - - - - 10pg 10 8 (80.0) 1 (10.0) - - 1 (10.0) - - SBA (W-135) . i i-r lμg 9 7 (77.8) - - - 1 (11.1) - - 4μg 8 7 (87.5) - - - - 1 (12.5) - 10μg 10 8 (80.0] - - 1 (10.0) - 1 (10.0) - 46 Table A-6: Stage II (Toddlers) - Distribution of SBA Titers at Baseline (Day 0) by TetraMenD Dosage Level (Per-Protocol Population) n* (%) of Participants with Titer-Result9 512 to 65536 Serogroup &dosage level tND° 512 1024 2048 4096 8192 16384 32768 65536 SBA (A) lμg 9 1 (11.1) - - - - - - 4μg 8 1 (12.5) - - - - 10μg 10 - - 1 (10.0) - - - - - SBA (C) lμg 9 - - - - - - - - 4μg 8 - - - - - - - - 10μg 10 - - - - - . |!i[" - - SBA (Y) lμg 9 - - - - - " - - 4μg 8 - - - - - - - - 10μg 10 - - - - - " - - SBA (W-135) 1 μg 9 1 (11.1) - - - - - - 4μg 8 - - - - - - - - 10μg 10 - - - - - " - - 47 Table A-7: Stage II (Toddlers) -Distribution of SBATiters60 DaysAfter the 1st Injection (Day 60), by TetraMenD Dosage Level Serogroup & dosage level ND601 n* (%) of Participants with Titer Result* SBA (A) lμg 9 - - - - 1 (11.1) 1 (11.1) 1 (11.1) 4μg 8 1 (12.5) - - -; ,., . lOμg 10 - - - - - - 1 (10.0) SBA (C) lμg 9 3 (33.3) 1 (11.1) - 1 (11 l) 2 (22.2) 1 (11.1) 4μg 8 1 (12.5) . - 2(25.0) 2(25.0) 1 (12.5) lOμg 10 2(20.0) - 1(10.0^ 1 (10.0) 220.0) 1 (10.0) SBA(Y) lμg 9 2(22 2 ) 1 (11 1) 2(22 2 ) 1 (111) 2(22 2) 1(11 1) 4μg 8 1(12 5) - 1(12 5) 1(12 5) 3(37 5 ) lOμg 10 4(40.0)i 2(20.0) 1 (10.0) 3 (30.0) - SBA (W-135) 1μg 9 5(55 6) - - 3(33 3 ) - 4μg 8 5 (62.5) - _ _ 1(12.5) 1(12.5) lOμg 10 2(20.0) - 1(10.0) 3 (30.0) - 48 Table A-7: Stage II (Toddlers) - Distribution of SBA Titers 60 Days After the 1st Injection (Day 60), by TetraMenD Dosage Level n* (%) of Participants with Titer Result Serogroup &dosage level Nn60« 512 1024 2048 4096 8192 16384 32768 65536 SBA (A) lμg 9 2 (22.2) - 4 (44.4) - - - - - 4μg 8 - - 4 (50.0) 2 (25.0) 1 (12.5) - - - 10μg 10 2 (20.0) - 5 (50.0) 2 (20.0) - - - - SBA(C) lμg 9 - - 1 (11.1) - - .,..,- - - 4μg 8 2 (25.0) - - - - - - - 10μg 10 1 (10.0) 2 (20.0) - - - - - SBA(Y) lμg 9 - - - - - - - - 4μg 8 - 2 (25.0) - - . - - 10μg 10 - - - - - - - - SBA (W-135) 1μg 9 - - 1 (11.1) - - - - 4μg 8 - - 1 (12.5) - - - - 10μg 10 3 (30.0) - 1 (10.0) - - - - 49 Table A-8: Stage II (Toddlers) - Distribution of SBA Titers 30Days After the 2nd Injection (Day 90), by TetraMenD Dosage Level n* (%) of Participants with Titer Result8 Serogroup & NDWI dosage level SBA (A) lμg 9 - - - - - - - 4μg 8 - - - - - - 10μg 10 - - - - - - - SBA (C) lμg 9 2 (22.2) - 1 (11.1) 1 (11.1) 2 (22.2) 1 (11.1) 4μg 8 - - - - 1(12.5) 2 (25.0) 1 (12.5) 10μg 10 3 (30.0) 1 (10.0) 1 (10.0) 2 (20.0) SBA(Y) 1μg 9 - - - 3 (33.3) - 2 (22.2) 1 (11.1) 4μg 8 1 (12.5) 2 (25.0) 1 (12.5) 10μg 10 1 (10.0) - 1 (10.0) 3 (30.0) 2 (20.0) 2 (20.0) SBA (W-135) lμg 9 1(11.1) 1(11.1) 1(11.1) 1 (01.1) 2 (22.2) 4μg 8 - - - - 1 (12.5) 1(12.5) 10μg 10 - - - 1 (10.0) 1 (10.0) 3 (30.0) 1 (10.0) 50 Table A-8: Stage II (Toddlers) - Distribution of SBA Titers 30 Days After the 2nd Injection May 90), by TetraMenD Dosage Level n* (%) of Participants with Titer Result* 512 to 65536 Serogroup & dosage level ND9o 512 1024 2048 4096 8192 16384 32768 65536 SBA (A) lμg 9 - - 8 (88.9) - 1 (11.1) > - - - 4μg 8 5 (62.5) 1 (12.5) 2 (25.0) 10 μg 10 2(20.0) ■ 4 (40.0) 4 (40.0) - - - - SBA (C) 1μg 9 1 (11.1) 1 (11.1) 4μg 8 2 (25.0) 2 (25.0) - - - - - 10μg 10 - 2 (20.0) 1 (10.0) - - - - - SBA(Y) Lμg 1 (11.1) 1 (11.1) 1 (11.1) - - - - - 4μg 8 2 (25.0) 1 (12.5) 1 (12.5) - - - - - 10μg 10 1 (10.0) - - - - - - - SBA (W-135) 1μg 9 - 2 (22.2) 1 (11.1) - - -» - - 4μg 8 4 (50.0) l(12.5) 1 (12.5) - - - - - 10 μg 10 1 (10.0) 1 (10.0] 2 (20.0) - ™ ■■ *i - - ■ 51 Table A-9: Baseline, Stage II 60 Days Post-Injection TetraMenD Dosage Achieving SBA Thresholds at #1, and 30 Days Post-Injection #2, by (Per-Protocol Population) Serogroup& dosage level ~T"DO/D60/ D9o Achievi Threshol >1:8 % Achieving Threshold >-l:16 Baseline ~0) Post-(D60) Post-(D90) Baseline~0) Post-(D60) Post-(D90) SBA A lμg 9/9/9 55.6 100.0 100.0 33.3 100.0 100.0 4μg 8/8/8 12.5 87.5 100.0 12.5 87.5 100.0 10 μg 10/10/10 20.0 100.0 100.0 20.0 100.0 100.0 SBA C lμg 9/9/9 0.0 66.7 77.8 0.0 55.6 77.8 4μg 8/8/8 12.5 100.0 100.0 12.5 87.5 100.0 10 pig 10/10/10 30.0 80.0 70.0 30.0 80.0 60.0 SBA Y 1 pig 9/9/9 55.6 77.8 100.0 44.4 77.8 100.0 4 pig 8/8/8 37.5 87.5 100.0 12.5 87.5 100.0 10μg 10/10/10 20.0 60.0 90.0 10.0 60.0 90.0 SBA W-135 Lμg 9/9/9 22.2 44.4 88.9 22.2 44.4 77.8 4μg 8/8/8 12.5 37.5 100.0 12.5 37.5 100.0 10 μg 10/10/10 20.0 80.0 100.0 20.0 80.0 100.0 52 Table A-9: Stage HBaseline, 60 Days Post-Injection -Proportions #1, and Dosage Achieving SBA30 Days Post-Injection #2, at by Serogroup& dosagelevel ND0/ND60/ND 90 %Achieving Threshold >.1:32 %Achieving Threshold >-l:64 Baseline ~0) Post-(D60)l Post-1D90) Baseline ~0) Post-(D60) Post-(D90) SBA Serogroup A Lμg 9/9/9 33.3 100.0 100.0 33.3 100.0 100.0 4μg 8/8/8 12.5 87.5 100.0 12.5 , 87.5 100.0 10 μg 10/10/10 20.0 100.0 100.0 10.0 100.0 100.0 SBA Serogroup C Lμg 9/9/9 0.0 55.6 66.7 0.0 44.4 66.7 4μg 8/8/8 12.5 87.5 100.0 12:5 87.5 100.0 10 μg 10/10/10 20.0 80.0 60.0 20.0 70.0 50.0 SBA Serogroup Y lμg 9/9/9 33.3 66.7 100.0 11.1 44.4 66.7 4|μg 8/8/8 0.0 75.0 100.0 0.0 ;. 75.0 87.5 10 μg 10/10/10 10.0 40.0 80.0 10.0 30.0 50.0 SBA Serogroup W-135 lμg 9/9/9 22.2 44.4 66.7 22:2 44.4 66.7 4μg 8/8/8 12.5 37.5 100.0 12.5 37.5 100.0 10 μg 10/10/10 20.0 80.0 100.0 10.0 70.0 90.0 53 Table A-10: Stage II (Toddlers) - SBA and IgG ELISA Results Among Toddlers by TetraMenD Dosage Level At Baseline, 60 Days Post-Injection #1, and 30 Days Post-Injection #2 (Per-Protocol Population) Sero-group &*level level NDO*D60"D90 GMT/GMC* (95% CI) Mean Fold 1" (from baseline) Fold1(from baseline) Baseline ~0) Post-Inj#l(D60) Post-Inj#2 (D90) Post-Inj #1 (D60) Post-Inj #2(D90) Post-Inj #1(D60) Post-Inj #2 (D90) SBA(A) lμg 9/9/9 17.3(3.9-77.0) 597.3 (214.5 1663.1) 2389.1 (1674.8 -3407.9) 34.6 138.2 100.0 100.0 4μg 8/8/8 8 7(1.4-55.1) 1328.0 (178.7 9870.5) 3158.4 (1857.4 -5370.7) 152.2 362.0 75.0 87.5 10 μg 10/10/10 9.2 (2.2-38.7) 1448.2 (740.0 2833.9) 2048.0(1155.2-3630.7) 157.6 222.9 90.0 90.0 SBA (C) lμg 9/9/9 4.0 (4.0-4.0) 29.6 (5.9-148.0) 69.1 (14.8 -322.6) 7.4 17.3 55.6 77.8 4μg 8/8/8 6.7 (2.0-23.0) 117.4 (37.7 -365.3} 304.4 (128.5 -721.1) 17.4 45.3 75.0 100.0 10 pug 10/10/10 8.0(3.4-18.6) 97.0 (22.9 -411.4) 68.6 (11.0-428.6) 12.1 816 80.0 50.0 SBA(Y) 1μg 19/9/9 10.9 (4.7-25.4) 34.6 (11.0-108.5) 174.2 (52.7 -575.2) 3.2 16.0 44.4 77.8 4μg 8/8/8 5.7 (3.7-8.8) 98.7 (20.4-478.0) 304.4(100.7 -920.1) 17.4 53.8 87.5 100.0 10 pug 10/10/10 5.7 (3.0-10.6) 14.9 (6.1-36.3) 48.5 (18.9 -124.3) 2.6 8.6 50.0 80.0 54 Table A-10: Stage II (Toddlers) - SBA and IgG ELISA Results Among Toddlers by TetraMenD Dosage Level At Baseline, 60 Days Post-Injection #1, and 30 Sero-gtoupMrdosage level N DO"D60/>S»0 GMT/GMC*(95%CI) Mean Fold (from baseline) ->4 Fold"t (frombaseline) Baseline(POl Post-Inj#l 60* Post-Inj#2(D90) Post-Inj #1 (D60) Post-Inj #2 (D90) Post-Inj^ (D60) Post-Inj #2 (D90) SBA (W-13 5) lμg 9/9/9 9.3 (2.4-36.1) 20.2 (3.7-108.7) 101.6 (18.1-571.0) 2.2 10.9 33.3 66.7 4μg 8/8/8 6.2(2.2-17.2) 22.6 (2.8-184.9) 430.5 (172.2 -1076.3) 3.7 69.8 37.5 100.0 10 μg 10/10/10 7.0 (2.9-16.6) 90.5 (20.2 -406.1) 274.4 (97.9 -769.2) 13.0 39.4 70.0 100.0 IgG ELISA (A) lpμg 9/9/9 0.3(0.1-0.7) 0.8(0.3-1.9) 1.9(0.6-6.0) 2.6 6.3 22.2 44.4 4pug 8/8/8 0.2 (0.1-0.4) 2.1 (0.9-4.8) 4.4 (2.1-9.1) 12.4 26.1 87.5 100.0 10 pug 10/10/10 0.2(0.1-0.3) 4.4 (2.9-6.5) 6.2(4.2-9.1) 23.4"" 33.1 100.0 100.0 IgG ELISA (C) lμg 9/9/9 0.1 (0.1-0.2) 0.3 (0.1-0.9) 0.5(0.2-1.3) 2.6 3.8 33.3 44.4 4 pig 8/8/8 0.2 (0.0-0.7) 1.0 (0.3-3.1) 1.5(0.6-3.6) 5.6 8.3 75.0 87.5 10 pig 10/10/10 0.2 (0.1-0.3) 0.7 (0.3-1.5) 1.2(0.7-2.0) 4.3 7.5 60.0 70.0 55 Table A-10: Stage U (Toddlers) - SBA and IgG ELISA Results Among Toddlers by TetraMenD Dosage Level At Baseline, 60 Days Post-Injection #1, and 30 Sero-groupdosage level •DO>D60>D90 GMT/GMC*(95% CI) Mean Fold (from baseline) %4FoId"t (from baseline) Baselinemm Post-Ini#l (P60) Post-Inj#2 (D90) Post-Ini#l (P60) Post-Ini#2(P90) Post-Ini#l (P60) Post-Ini#2(D90) IgG ELISA (Y) 1μg 9/9/9 0.4 (0.2 0.6) 0.7 (°0 (o824) 1.9 3.8 11.1 33.3 4 μg 8/8/8 0"3 (0.2-0.4) 1.2 (0.5-2 8) 4"5 (2.7-7.6) 4.4 16.4 37.5 100.0 10pug 10/10/10 (0.1o0.3) 0.8(0.4-1.3) 1.84.5) 4.3 10.2 70.0 90.0 IgG ELISA (W-135) 1μg 9/9/9 0.2 (0.1-0.3) 0.3 (0.2--0.5) 0.8 1.9 5.2 22.2 55.6 4μg 8/8/8 0.1 (0.1-0.2) 0.6 (0.2- 1.5 8-(0:) 5.3 12.7 62.5 100.0 10 pig 10/10/10 (0 2) 0.50.9) 8.2(0 2) 4.5 11.8 60.0 80.0 Day 0: Baseline blood sample drawn prior to injection #1. Day 60: Blood sample drawn 60 days following injection #1 and prior to injection #2. Day 90: Blood sample drawn 30 days following injection #2. % 4-fold rise: Post-Inj #1: the percentage of toddlers which had a 4-fold rise in GMT at day 60 in comparison to day 0; Post-Inj #2: the percentage of toddlers which had a 4-fold rise in GMT at day 90 in comparison to day 0. N: number of evaluable participants *GMTs are computed for the SBA data; GMCs are computed for the IgG ELISA data. Table A-l 1 summarizes the GMT by Dose, Patient Age and Serogroup Table A-ll Summary of GMT by Patient Age and Serogroup Age Dose TetraMenD No. of Subjects Blood Day A GMT CGMT WGMT YGMT 12 4μg 4 0 13.45 4.00 4.00 4.00 4μg 4 60 1448.15 107.63 32.00 53.82 4μg 4 90 4096.00 215.27 724.08 304.44 10 μg 6 0 16.00 12.70 10.08 4.00 56 10μg 6 60 1448.15 64.00 101.59 12.70 10 μg 6 90 2298.80 80.63 256.00 40.32 13 4μg 1 0 4.00 4.00 4.00 16.00 4 μg 1 60 4.00 64.00 , 4.00 128.00 4μg 1 90 2048.00 64.00 512.00 128.00 10 μg 1 0 4.00 4.00 4.00 64.00 10μg 1 60 4096.00 256.00 512.00 4.00 10 μg 1 90 4096.00 1024.00 1024.00 16.00 14 10 μg 2 0 4.00 4.00 4.0000 5.66 10 μg 2 60 724.08 181.02 128,00 32.00 10μg 2 90 1024.00 5.66 512.00 128.00 15 4μg 2 0 90.51 4.00 4.00 5.66 4μg 2 60 2896.31 45.25 32.00 256.00 4μg 2 90 2896.31 362.04 181.02 362.04 16 4μg 2 0 4.00 4.00 4.00 4.00 4μg 2 60 2896.31 90.51 4.00 45.25 4μg 2 90 4096.00 256.00 256i00 128.00 18 4 μg 1 0 4.00 256.00 128,00 8.00 4μg 1 60 2048.00 512.00 2048.00 1024.00 4μg 1 90 2048.00 1024.00., ,2048.00 2048.00 10μg 1 0 4.00 4.00 4.00 4.00 10 μg 1 60 2048.00 128.00 4.00 32.00 10 μg 1 90 2048.00 256.00 32.00 64.00 Stage III Dosage Study in Infants This Clinical Trial is an unblinded open level –dose escalation trial three doses level of TetraMenD vaccine, which is administered to participants in three age groups. In Stage III, 5 ninety healthy infants (6 to 12 weeks of age) receive three injections of a single dosage level of TetraMenD vaccine. Infant participants received TetraMenD injections at age 2 months (injection #1), at age 4 months (injection #2), and at age 6 months (injection #3). Serum specimens for serologic analysis are obtained at two time points: at age 6 months (2 months following injection #2), and at age 7 months (one month after injection #3). All available specimens are analyzed for SBA against meningococcal polysaccharide serogroups A, C, Y, and W-135, and by ELISA for IgG antibody against these same serogroups. The SBA and IgG ELISA findings for all serogroups are summarized below. The results are summarized in the following Tables. 57 Table A-13: Stage III (Infants) - Distribution of SBA Titers at Age 7 months (one month post 3rd dose), by TetraMenD Dosage Level (Per-Protocol Population) n* (%) of Participants with Titer Result & dosageSerogrouiWj N7mt 512 1024 2048 4096 8192 16384 32768 65536 SBA (A) lμg 23 3 (13.0) 2 (8.7) 4μg 24 3 (12.5) 3 (12.5) _ _ _ _ _ _ lOμg 21 - 2 (9.5) - - - - - - SBA (C) 1pg 23 - 1 (4.3) - - - - - - 4pg 24 1(4.2) - - - - - - 10μg 21 1 (4.8) - - - - - - SBA(Y) -,. 1μg 23 1 (4.3) - - - - - - 4pg 24 - - - - - - - 10μg 21 1 (4.8) - - - - - - SBA (W-135) lμg 23 - - (4.J3) - - - - - 4pg 24 - - - - - - - 10μg 21 1(4.8: 1 - - - - - - 59 Table A-14: Stage m (Infants) - Proportions Achieving SBA Thresholds at Age 6 months (pre 3rd dose) and at Age 7 months (post 3rd dose) by TetraMenD Dosage Level (Per-Protocol Population) Serogroup&dosagelevel N6in T % Achieving Threshold I >-l:8 >-l:16 >1:32 >-l: 64 6 mos 7 mos 6 mos 7 mos 6 mos 7 mos 6 mos 7 mos SBA (A) lμg 22/23 54.5 78.3 36.4 65.2 27.3 56.5 13.6 47.8 4μg 23/24 69.6 91.7 69.6 91.7 56.5 83.3 30.4 75.0 10 μg 21/21 85.7 85.7 66.7 85.7 52.4 762 19.0 61.9 SBA (C) 1μg 22/23 54.5 78.3 50.0 73.9 45.5 60.9 40.9 52.2 4μg 23/24 60.9 54.2 52.2 50.0 47.8 45.8 43.5 37.5 10 μg 21/21 85.7 7L4 81.0 66.7 71.4 66.7 61.9 52.4 SBA(Y) lμg 22/23 40.9 69.6 27.3 60.9 18.2 47.8 9.1 30.4 4μg 23/24 34.8 66.7 26.1 54.2 21.7 54.2 21.7 33.3 10 WJ 21/21 47.6 81.0 42.9 76.2 23.8 52.4 4.8 333 SBA (W-135) lμg 22/23 27.3 78.3 18.2 73.9 4.5 60.9 4.5 47.8 4μg 23/24 30.4 62.5 21.7 45.8 17.4 37.5 83 33.3 10 μg 21/21 42.9 76.2 38.1 762 23.8 61.9 19.0 47.6 ants at each time point (6 months ofage; 7 months of age N: number of evaluable participants Table A-15: Stage m (Infants) - SBA and IgG ELISA Results Among Infants At Age 6 months (pre 3rd dose) and at Age 7 months (post 3rd dose), by TetraMenD Dosage Level (Per-Protocol Population) & dosage1»V Age 6 mos Age 7 mos SBA (A) lμg 22/23 11.3 (6.2-20.6) 40.7 (17.6-94.0) 4μg 23/24 25.1 (12.9-49.0) 101.6 (51.9-199,0) 10 μg 21/21 18.9 (12.2-29.1) 68.4 (32,2-145.1) 60 Table A-15: Stage III (Infants) - SBA and IgG ELISA Results Among Infants At Age 6 months (pre 3rd dose) and at Age 7 months (post 3rd dose), by TetraMenD Dosage Level (Per-Protocol Population) Serogroup& dosagelevel N6m/N7m GMT/GMC :* (95% CI) Age 6 mos Age 7 mos SBA (C) lμg 22/23 19.3 (9.3-40.1) 37.2 (18.6-74,5) 4μg 23/24 24.4 (11.0-54.1) 19.6 (9.4-40.6) 10 μg 21/21 43A (23.2-80.0) 35.3 (16.6-75.2) SBA(Y) .!■" lμg 22/23 7.8 (5.0-1L9) 21.0 (11.0-40.0) 4μg 23/24 8.5(5.0-14.4) 19.6 (10.7-35,7) 10 μg 21/21 9.1 (5.9-14.2) 26.3; (142-48.6) SBA (W-135) lμg 22/23 5.8 (4.2-8.1) .35.0(17.3-71.1) 4μg 23/24 6.9 (4.6-10.4) 17.4 (9A-33.5) 10 μg 21/21 9.8 (5.6-16.9) 34.2 (17.0-683) IgG ELISA (A) lμg 22/22 0.5 (0.4-0.6) 0.5 (0,4-0.6) 4μg 21/21 0.7 (0.4-1.3) 0.8 (0.5-1.3) 10 μg 19/19 1.3 (1.0-1.8) 13 (0.8-2.1) IgG ELISA (C) lμg 21/21 0.5 (0.4-0.8) 0.7 (0.5-0.9) 4μg 21/21 0.4 (0.3-0.7) ,.,0.8 (0.5-1.1) 10 μg 19/19 1.1 (0.8-1.6) 1.2 (0.7-2.0) 61 Table A-15: Stage III (Infants) - SBA and IgG ELISA Results Among Infants At Age 6 months (pre 3rd dose) and at Age 7 months (post 3rd dose), by TetraMenD Dosage Level (Per-Protocol Population) Serogroup& dosagelevel N6m/N7m GMT/GMC* (95% CI) Age 6 mos Age 7 mos IgG ELISA (Y) lμg 20/20 0.5 (0.3-0.8) 1.2 (0.8-1.6) 4μg 20/21 0.7 (0.4-1.2) 1.0 (0.6-1.8) 10 μg 18/19 1.2 (0.8-1.8) 1.8 (1.1-3.1) IgG ELISA (W-135) lμg 20/20 0.5 1.1(0 8-.1) 4μg 20/21 0.5 (0.3-0.9) 0.9 (0.6-1.3) lOμg 18/19 0.9. (0.7-1.3) 1.5 (0.8-2.5) Table A N: number of evaluable participants *GMTs are computed for the SBA data; GMCs are computed for the IgG ELISA data. ■16 presents a summary of GMT by patient age and serogroup Table A-16 Summary of GMT by Patient Age and Serogroup 1 Age (weeks) DoseTetraMenD No. of Subjects Blood Day A GMT C GMT W GMT Y GMT 7 4μg 1 6-12 weeks 512.00 128.00 4.00 4.00 4μg 1 6 month 512.00 128.00 4.00 32.00 8 lμg l 6-12 weeks 4.00 4.00 4.00 4.00 1μg 1 6 month 32.00 16.00 16.00 4.00 4μg 6 6-12 weeks 11.31 7*13 5.66 4.49 4μg 6 6 month 71.84 7.13 22.63 6.35 10 μg 1 6-12 weeks 9.51 19.03 5.66 9.51 10- μg 1 6 month 32.00 38.05 19.03 32.00 9 lμg 13 6-12 weeks 11.02 18.78 5.51 7.58 62 lμg 14 6 month 55.17 55.17 40.99 22.63 4μg 13 6-12 weeks 30.34 27.27 7.19 14.38 4μg 13 6 month 60.66 19.80 14.38 27.27 10μg 6-12 weeks 21.53 ,35.33 10.25 7.61 10μg 6 month 70.66 26.25 26.25 22.63 10 1 μg 10 6-12 weeks 19.70 29.86 12.13 7.46 1 μg 10 6 month 39.40 19.70 45.25 14.93 4μg 6-12 weeks 12.13 32.00 4.00 4.00 4μg 6 month 114.04 22.63 28.51 25.40 10μg 6-12 weeks 19.50 43.07 8.00 14.49 10μg 6 month 52.50 35.33 39.01 32.00 11 l μg 6-12 weeks 4.00 4.00 4.00 16.00 1 μg 6 month 8.00 4.00 4.00 32.00 4μg 6-12 weeks 512.00 512.00 64.00 64.00 4μg 6 month 1024.00 256.00 128.00 128.00 12 4μg 6-12 weeks 32.00 4.00 4.00 64.00 4μg 6 month 1024.00 64.00 256.00 256.00 13 10 μg 6-12 weeks 512,00 45.25 64.00 22.63 10μg 1 6 month 724.08 90.51 256.00 181.02 63 Pediatric Vaccines Administered Concomitantly with TetraMenD in Infants Infants currently receive routine pediatric vaccinations per current ACIP recommendation and local practice. In this study, infants receive TetraMenD with pediatric vaccinations. DTacP (Tripedia®) and Hib (ActHIB®) are administered at ages 2,4, and 6 months. Either IPV or OPV may be given; IPV is administered with the first and second injections of TetraMenD (at ages 2 and 4 months). Hepatitis B vaccine is given per local practice; hepatitis B vaccine is administered at age 2 months to some participants, but not administered to any participant at ages 4 months or 6 months. During the conduct of the infant stage of this trial, RotaShield® became licensed and received an ACIP recommendation for routine use. A single participant received RotaShield® at ages 4 months and 6 months in the context of this trial. ... Antibody responses to routinely administered pediatric vaccine antigens are assessed at age 6 months and 7 months. The results are summarized in separate Tables. Infants participating in this trial received DTacP and PRP vaccines at 2,4, and 6 months of age; the 7-month blood draw occurred one month after the third injection of these vaccines. For each of these vaccine antigens (diphtheria, tetanus, pertussis FHA, pertussis PT, and PRP), the observed antibody levels do not demonstrate a statistically significant difference among the 3 TetraMenD dosage groups (all p-values >0.05). (See Table A-17) In the context of this trial, IPV is administered at 2 months and at 4 months of age. The 7-month blood draw occurs three months after the second injection of IPV. For polio type 1 and polio type 2, the observed GMTs, proportions with NA _>1:4, and proportions with NA _> 1:8 do not demonstrate a statistically significant difference among the 3 TetraMenD dosage groups (all p-values >0.05). At least 95.0% of all 3 TetraMenD dosage groups demonstrate protection against polio types 1 and 2 by proportion with NA >_1:8. For polio type 3, the GMTs in the 1 ug, 4 ug, and 10 gg groups are 562.7,164.0, and 113.3, respectively. The difference among the groups in the polio type 3 GMTs is statistically significant (p=0.001, ANOVA). However, all three TetraMenD dosage groups demonstrate protection against polio type 3 by proportion with NA >_1:8 (100.0% [22/22], 100.0% [21/21], and 94.1% [16/17], respectively). These proportions are not statistically different (p=0283, Fisher"s exact test). Moreover, the observed GMTs for the three polio serotypes 64 are well within published ranges following two doses of IPV at 2 and 4 months of age, the IPV vaccination schedule utilized in this trial. The 7-month blood draw occurs at a minimum of 5 months after the most recent hepatitis B vaccination. The observed levels of hepatitis B surface antibody by GMT and proportion >10 mlU/mL do not demonstrate a statistically significant difference among the 3 TetraMenD dosage groups (both p-values —>0.649). Notably, no infants in this trial received hepatitis B vaccine at the 6-month visit, which is the earliest recommended age for the third dose of this vaccine. This may explain why the proportions of 7-month-old infants with hepatitis B surface antibody titers >-10 mlU/mL are consistent with published ranges for detectable antibody following the initial doses of the vaccine, but lower than would have been expected for protective antibody levels following the complete three-vaccination series. The results of this Study are summarized in the following Tables. Table A-17: Stage HI (Infants) - Immunogenicity of Concomitant Vaccines Among Infants At Age 7 Months, by TetraMenD Dosage Level (Per-Protocol Population) __ Antigen &ImmunologicCriteria N7m pWlO TetraMenD Dosage Level p-value* lμg 4gg 10 gg Diphtheria (IU/mL) GMT (95% CI 23/23/2 1 0.16(0.10 -0.25) 0.09(0.06 -0.14) 0.08(0.05 -0.15) 0.150 %->0.01 100.0 100.0 95.2 0.313 %->0.10 56.5 43.5 47.6 0.750 Tetanus (IU/mL) GMT (95% CI) 23/24/2 1 1.52(1.08-2.15) 1.26(0.88 -1.78) 1.23(0.88 -1.74) 0.618 % ->0.01 100.0 100.0 100.0 Not calculable %>-0.10 100.0 100.0 100.0 Not calculable Pertussis FHA ELISA GMC (95% CD 20/20/1 9 81.6(61.4 -108.4) 69.6T55.6 -87.2) 63.4C43.5 -92.3) 0.455 65 Table A-17: Stage m (Infants) - Immunogenichy of Concomitant Vaccines Among Infants At Age 7 Months, by TetraMenD Dosage Level (Per-Protocol Population) Antigen & ImmunologicCriteria N7m1μg14μg110 TetraMenD Dosage Level p-value* lμg 4μg 10 μg Pertussis PT ELISA (EU/mL) GMC (95% CD 20/21/1 9 66.4(43.6 -101.2) 56.5(37.2 -85.8) 80.0(56.7 -...112.7) 0.441 Pertussis PT CHO (titer) GMT MS% CI) 20/20/1 6 222.9(130.8-379.6) 256.0(175.2-374.2) 332.0(200.9 -548.7) 0.476 Polio type 1 (titer) GMT (95% CI) 22/22/2 0 169.9 (95.3 -303.0) 122.1 (72.6 -205.4) 93.7 (46.5 -188.7) 0.350 %NA>-1:4 100.0 100.0 100.0 Not calcu lable %NA>-1:8 100.0 95.5 95.0 0.760 Polio type 2 (titer) GMT (95% CI) 22/21/1 8 183.9 (96.2 -351.4> 220.7 (135.9-358.5^ 211.2 (107.3 -415.6^ 0.893 %NA>-1:4 100.0 100.0 :!, 100.0 Not %NA>-1:8 100.0 100.0 100.0 Notcalculable Polio type 3 (titer) GMT (95% CI) 22/21/1 7 562.7(363.3 -871.8) 164.0 (97.8 -274.8) 113.3 (44.6* 287.7) 0.001f %NA>-1:4 100.0 100.0 94.1 0.283 %NA>-1:8 100.0 100.0 94.1 0.283 PRP(ug/mL) GMT (95% CI) 23/22/1 9 4.87 (3.04-7.78) 4.41 (2.52 -7.69) 3.39(1.64-6.99) 0.648 %>.0.15 100.0 100.0 100.0 Not calculable % >-1.0 ug/mL 95.7 81.8 78.9 0.209 66 Table A-17: Stage m (Infants) - Immunogenicity of Concomitant Vaccines Among Infants At Age 7 Months, by TetraMenD Dosage Level (Per-Protocol Population) 48.3 (28.1 - 83.2) 89.5 46.9 (12.9 -170.1) 81.0 * GMT comparisons use the F-test. Comparisons of percentages use the Fisher"s exact test. t p-value Antigen & Immunologic. Criteria N7m lμg/4 μg/10 μg — Hep B Surface Ab (mlU/mL) GMT (95% CI) 21/23/1 9 TetraMenD Dosage Level 1 μg 4 μg 10 μg 36.9 (12.4 -110.2) 78.3 p-value* 0.916 0.649 Example 11 Study B One and Six Month Study in Children Aged 2 to 10 This is a randomized, active-controlled sutyd of healthy children between the ages of 2 and 10, comparing a single dose of TetraMenD with a single dose of Menomune. Blood specimens are drawn on DO, before vaccination, D28 and at 6-months post DO. The overall safety of TetraMenD compared with Menomune is comparable. The results of this study are summarized in the following Tables. Distribution of SBA-BR Antibody Titers Table B-l shows the frequency distribution of baseline, Day 28 and Month 6 SBA-BR antibody titers for each serogroup. Table B-l: Distribution of SBA-BR Antibody Titers at Day 0, Day 28, and Month 6 AfterVaccination (Per-Protocol Population) SBA-BR Titers Test Test Date GroupP(N) SBA(A) DayO TetraMenD (638) 280 (43.9) 20 (3.1) 15 (2.4) 24 (3.8) 44 (6.9) 63 (9.9) 64 (10.0) 56 (8.8) Menomune(655) 281 (42.9) 26 (4.0) 12 (1.8) 52 (7.9) 43 (6.6) 64 (9.8) 49 (7.5) 56 (8.5) 67 Table B-1: Distribution of SBA-BR Antibody Titers at Day 0, Day 28, and Month 6 AfterVaccination (Per-Protocol Population) SBA-BR Titers Test Test Date Groupn/Kh Day28 TetraMenD(637) 3 (0.5) 0 (0.0) 2 (0.3) 4 (0.6) 11 (1.7) 30 (4.7) 35 (5.5) 69 (10.8) Menomune (654) 11 (1.7) 6 (0.9) 3 (0.5) 8 (1-2) 18" (2.8) 45 (6.9) 66 (10.1) 90 (13.8) Month 6 TetraMenD (607) 17 (2.8) 6 (1.0) 1 (0.2) 9(1.5) 16 (2.6) 31 (5.1) 52 (8.6) 64 (10.5) Menomune (623) 99 (15.9) 13 (2.1) 15 (2.4) 23 (3.7) 29 (4.7) 52 (8.3) 70 (11.2) 99 (15.9) 68 Table B-1: Distribution of SBA-BR Antibody Titers at Day 0, Day 28, and Month 6 AfterVaccination (Per-Protocol Population) SBA-BR Titers Test Test Date GroupP~) SBA(C) Day 0 TetraMenD(638) 339(53.1) 30 (4.7) 18 (2.8) 30 (4.7) 31 (4.9) 51 (8.0) 61 (9.6) 37 (5.8) Menomune(655) 368 (56.2) 34 (5.2) 12 (1.8) 21 (3.2) 43 (6.6) 54 ( 8.2) 51 (7.8) 25 (3.8) Day 28 TetraMenD (636) 24(3.8) 10(1.6) 13 (2.0) 27 (4.2) 44 (6.9) 85 (13.4) 102(16.0) 97 (15.3) Menomune(653) 69(10.6) 10(1.5) 6 (0.9) 34 (5.2) 55 ( 8.4) 87 (13.3) 90 (13.8) 96(14.7) Month 6 TetraMenD(607) 85 (14.0) 19 (3.1) 17 (2.8) 35. (5.8) 67 (11.0) 90 (14.8) 88(14.5) 66 (10.9) Menomune(623) 185 (29.7) 30 (4.8) 14 (2.2) 35 (5.6) 54 (8.7) 68 (10.9) 61 (9.8) 73 (11.7) 69 Table B-1: Distribution of SBA-BR Antibody Titers at Day 0, Day 28, and Month 6 AfterVaccination (Per-Protocol Population) SBA-BR Titers Test Type Test Date Group ~ ) SBA(Y) DayO TetraMenD (637) 88 (13.8) 13 (2.0) 17 (2.7) 40(6.3) 82 (12.9) 113 (17.7) 107 (16.8) 68 (10.7) Menomune(654) 96 (14.7) 11 (1.7) 12 (1.8) 42 (6.4) 81 (12.4) 116 (17.7) 124 (19.0) 66 (10.1) Day 28 TetraMenD (636) 11 (1.7) 3 (0.5) 5 (0.8) 8 (1-3) 19 (3.0) 69 (10.8) 100 (15.7) 121 (19.0) Menomune(654) 16 (2.4) 4 (0.6) 7 (1.1) 20 (3.1) 43 (6.6) 85 (13.0) 121 (18.5) 102 (15.6) Month 6 TetraMenD (608) 25 (4.1) 3 (0.5) 3 (0.5) 17 (2.8) 23 (3.8) 46 (7.6) 72 (11.8) 110 (18.1) Menomune (622) 62 (10.0) 17 (2.7) 7 (1.1) 24 (3.9) 38 (6.1) 73 (11-7) 98 (15.8) 114 (18.3) 70 WO 2004/103400 PCT/US2004/014466 ti Table B-1: Distribution of SBA-BR Antibody Titers at Day 0, Day 28, and Month 6 After Vaccination (Per-Protocol Population) SBA-BR Titers Test Type Test Date Group (N) SBAfW 135) DayO TetraMenD (638) 401 (62.9) 28 (4.4) 24 (3.8) 21 (3.3) 51 (8.0) 45 (7.1) 43 (6.7) 15 (2.4) Menomune (654) 403 (61.6) 36 (5.5) 22 (3.4) 30 (4.6) 52 (8.0) 48 (7i3) 34 (5.2) 17 (2.6) Day28 TetraMenD (636) 22 (3.5) 2 (0.3) 1 (0.2) 9 (1.4) 24 (3.8) 39 (6,1) 73 (11.5) 108 (17.0) Menomune(653) 43 (6.6) 3 (0.5) 4 (0.6) 8 (1.2) 33 (5.1) 61 (9.3) 88 (13.5) 130 (19.9) Month 6 TetraMenD(607) 46 (7.6) 9 (1.5) 3 (0.5) 10 (1.6) 31 (5.1) 69 (11.4) 96 (15.8) 107 (17.6) Menomune (624) 82 (13.1) 12 (1.9) 11 (1.8) 23 (3.7) 66 (10.6) 111 (17.8) 120 (19.2) 100 (16.0) Table B-1: Distribution of SBA-BR Antibody Titers at Day 0, Day 28, and Month 6 AfterVaccination (Per-Protocol Population) SBA-BR Titers 1024 to >65536 Test Test Date Grou"p(N) 1024 n(%o) 2048n (%) 4096n (%) 8192 n (%) 16384n (%) 32768 n (%) 65536 n(%o) >65536 n(%o) SBAfA) DayO TetraMenD (638) 40 (6.3) 26 (4.1) 2 (0.3) 3 (0.5) 1 (0.2) 0 (0.0) 0 (0.0) 0 (0.0) Menomune(655) 51 (7.S) 19 (2.9) 0 (0.0) 1 (0.2) 1 (0.2) 0 (0.0) 0 (0.0) 0 (0.0) Day 28 TetraMenD(637) 120 (18.8) 151 (23.7) 79 (12.4) 71 (11.1) 39 (6.1) 20 (3.1) 1(0.2) 1(0.2) Menomune (654) 122 (18.7) 162 (24.8) 62 (9.5) 44 (6.7) 16 (2.4) 1 (0.2) 0 (0.0) 0 (0.0) Month 6 TetraMenD (607) 129 (21.3) 139 (22.9) 48 (7.9) 52 (8.6) 27 (4.4) 16 (2.6) 0 (0.0) 0 (0.0) Menomune (623) 94 (15.1) 93 (14.9) 17 (2.7) 9(1.4) 8(1.3) 2 (0.3) 0 (0.0) 0 (0:0) Table B-1: Distribution of SBA-BR Antibody Titers at Day 0, Day 28, and Month 6 AfterVaccination (Per-Protocol Population) SBA-BR Titers 1024 to >65536 Test Type Test Date Group. ~) 1024n (%) 2048n(%) 4096n (%) 8192n (%) 16384n(%) 32768n(%) 65536n (%) >65536■ (%) SBA(C) DayO TetraMenD (638) 22 (3.4) 16 (2.5) 3 (0.5) 0 (0.0) 0 (0.0) 0 (0.0) 0 (0.0) 0 (0.0) Menomune(655) 20 (3.1) 22 (3.4) 3 (0.5) 0 (0.0) 1(0.2) 1(0.2) 0 (0.0) 0 (0.0) Day 28 TetraMenD (636) 95 (14.9) 92 (14.5) 19 (3.0) 16 (2.5) 6 (0.!9) 6 (0.9) 0 (0.0) 0 (0.0) Menomune (653) 86(13.2) 91 (13.9) 10 (1.5) 9 (1.4) 7 (1.1) 3 (0.5) 0 (0.0) 0 (0.0) Month 6 TetraMenD (607) 62 (10.2) 56 (9.2) 17 (2.8) 3 .(0.5) 1 (0.2) 1 (0.2) 0 (0.0) 0 (0.0) Menomune (623) 42 (6.7) 45 (7.2) 6(i.o) 7 (1.1) 1 ( 0.2) 1 (0.2) 1(0.2) 0 (0.0) 72 Table B-1: Distribution of SBA-BR Antibody Titers at Day 0, Day 28, and Month 6 AfterVaccination (Per-Protocol Population) SBA-BR Titers 1024 to >65536 Test Type Test Date Group M 1024■ (*) 2048■(%) 4096■(%)■ 8192n(%) 16384 32768 65536 >65536 SBAm DayO TetraMenD(637) 62 (9.7) 37 (5.8) 5 (0.8) 2 (0.3) 3 (0.5) 0 (0.0) 0 (0.0) 0 (0.0) Menomune (654) 50 (7.6) 43 (6.6) 10 (1.5) 2 (0.3) 1 (0-2) 0 (0.0) 0 (0.0) 0 (0.0) Day 28 TetraMenD (636) 111 (17.5) 113 (17.8) 29 (4.6) 21 (3.3) 17,,,, (2.7) 9 ( 1-4) 0 (0.0) 0 (0.0) Menomune (654) 127 (19.4) 86 (13.1) 23 (3.5) 13 (2.0) 5 (0.8) 2 (0.3) 0 (0.0) 0 (0.0) Month TetraMenD (608) 123 (20.2) 111 (18.3) 34 (5.6) 22 (3.6) 13 (2.1) 6 (1.0) 0 (0.0) 0 (0.0) 6 Menomune(622) 80 (12.9) 84 (13.5) 13 (2.1) 7 (1.1) 3 ... (0.5) 2 (0.3) 0 (0.0) 0 (0.0) 73 Table B-1: Distribution of SBA-BR Antibody Titers at Day 0, Day 28, and Month 6 AfterVaccination (Per-Protocol Population) SBA-BR Titers 1024 to >65536 Test TestDate Group~) 1024n(%) 2048n(%) 4096n(%) 8192n(%) 16384n (%) 32768n(%) 65S36n(%) >65536n(%) SBA135) DayO TetraMenD (638) 4 (0.6) 5 (0.8) 1 (0.2) 0 (0.0) 0 (0.0) 0(p.o) 0 (0.0) 0 (0-0) Menomune (654) 6 (0.9) 3 (0.5) 2 (0.3) 0 (0.0) 1(0.2) 0 (0.0) 0 (0.0) 0 (0.0) Day28 TetraMenD (636) 108 (17.0) 160(25.2) 36(5.7) 32 (5.0) 16 (2.5) 6 (0.9) 0 (0.0) 0 (0.0) M«nnmnni> (653) 117(17.9) 129(19.8) 24(3-7) a (1.4) 3 (0.5) 1 (P.2) 0 (0.0) 0 (0.0) Month 6 TetraMenD(607) 101 (16.6) 92 (15.2) 16 (2.6) 16. (2.6) 8 3 (0.5) 0 (0.0) 0 (0.0) Menomune (624) 67 (10.7) 25 (4.0) 5 2 (0.8) (0.3) 0. (0.0) 0 (0.0) 0 (0.0) 0 (0.0) Table B-2 summarizes of Geometric Mean Titer (GMT) by Subject Age and Serogroup for TetraMenD Table B-2 Summary of GMT by Subject Age and Serogroup for TetraMenD Age (in Year) Blood Day No. of Subjects SerogroupAGMT Serogroup CGMT SerogroupWGMT SerogroupY-135GMT 2 DayO 264 20.59 16.04 8.75 91.23 Day 28 260 940.26 151.41 332.43 393.88 6 Month 244 460.92 64.92 153.52 312.95 3 DayO 235 33.84 14.60 12.64 148.78 Day 28 228 1610.74 292.64 795.64 662.97 6 Month 228 1033.38 105.69 408.85 631.50 4 DayO 35 74.99 29.56 9.95 128.00 Day 28 34 3479.60 795.86 1731.22 906.10 6 Month 29 3812.58 302.62 634.88 908.65 5 DayO 27 118.51 32.00 29.63 121.59 Day 28 27 3010.02 612.79 1323.71 1050.63 6 Month 27 3010.02 406.37 679.07 948.10 6 DayO 38 38.40 34.42 13.83 112.66 Day 28 37 441432 950.07 2086.73 898.15 6 Month 37 3729.75 386.57 1005.00 849.06 7 DayO 30 111.43. 78.79 16.00 .,.., 111.43 Day 28 29 3999.26 1612.60 1691.56 153733 6 Month 28 2375.94 524.83 1049.67 1638.97 8 0ayO 18 118.51 54.86 1728 188.13 74 Day 28 16 6049.08 1878.02 2543.32 1069.34 6 Month 17 2837.86 453.05 1111.00 1418.93 9 DayO 29 116.33 91.60 21.31 87.32 Day 28 28 4870.99 2825.49 3119.59 "" 1521.66 6 Month 28 3995.85 974.54 1187.97 1412.75 10 DayO 21 98.30 27.13 18.26 45.25 Day 28 21 4233.45 3251.00 2337.06 1333.45 6 Month 20 3821.70 989.12 1782.89 1499.22 Table B-3shows the numbers and proportions of participants with a >4-fold rise in SBA-BR titer from baseline to Day 28 for the serogroups A, C, Y, and W-135. For each serogroup, these percentages are higher in the TetraMenD group than in the Menomune:* group. The differences in the proportions are: -0.0397, -0.0452, -0.1092 and -0.0562* for serogroups A, C, Y, and W-135, respectively. Table B-3: Summary of Primary Hypothesis Testing for the Per-Protocol Population Setogtoup >_ 4-fold rise in SBA titer TetraMenD n/N Pt Menomune®n/N Pm Difference (Pm - Pt) Upper One-sided95%CL of theDifference Serogroup A 558/636 0.8774 547/653 0.8377 -O;0397 -0.0077 Serogroup C 466/635 0.7339 449/652 0.6887 -0.0452 -0.0037 Serogroup Y 359/634 0.5662 298/652 0.4571 -0.1092 -0.0636 Serogroup W-135 578/635 0.9102 556/651 0.8541 -0.0562 -0.0267 n: number of participants with a >_ 4-fold rise from baseline titer N: total number of participants in the used population. Pt and Pm: proportions of participants with a 4-fold rise in SBA post-vaccination titer from the TetraMenD and Menomune® groups, respectively. The proportion of participants with SBA antibody titers > 32 at Day 28 after vaccination is 10 summarized in Table B-3. 75 Table B-3: Percentage and Number of Participants with an SBA-BR Antibody Titer 32 at 28 (Per-Protocol Day Day Post-Vacci Population) Nation TetraMenD%* 95% CI for (n"/N*) the percentage Menomune®% 95% CI for (»/N) tne percentage Serogroup A 99.22 f632I 637) (98.18,100.00) 96.94 (634 / 654) ( 95.32,100.00) Serogroup C 92.61 (589/ 636) ( 90.29,100.00) 86.98 (568 / 653) (84.16,100.00) Serogroup Y 97.01 (617/ 636) ( 95.37,100.00) 95.87 (627 / 654) (94.05,100.00) Serogroup W-135 96.07 (611/ 636) ( 94.25,100.00) 92.34 (603 / 653) (90.03,100.00) *%: t n: number of participants with titer>32 at Day 28 post-vaccination. t N: total number of participants with valid blood sample at Day 28 in this group. The proportion of participants with SBA antibody titers > 128 at Day 28 after vaccination is summarized in Table B-4. Table B-4: Percentage and Number of Participants with an SBA-BR Antibody Titer > 128 at Day 28 Post-Vaccination (Per-Protocol Population) TetraMenD%* 95% CI for (n"/N") the percentage Menomune* * 95% CI for %(Bt/N)the percentage Serogroup A Serogroup C Serogroup Y Serogroup W-135 96.86 (95.19,100.00)(617 / 637)81-45 (78.20,100.00)(518/ 636)92.77 (90.47,100.00)(590 / 636)90-88 (88.37,100.00)(578 / 636) 92.97 (90.73,100.00)(608 / 654)73.35 ( 69.79> 100.)(479 / 653)86.24 ( 83.36,100.00)(564/ 654)86.06 ( 83.17,100.00)(562/653) 76 Table B-4: Percentage and Number of Participants with an SBA-BR Antibody Titer > 128 at Day 28 Post-Vaccination (Per-Protocol Population) TetraMenD Menomune* %* 95/o CI for (n"/N) the percentage %* 95/o CI for (n«/N# the percentage *%: t n: number of participants with titer_128 at Day 28 post-vaccination. % N: total number of participants with valid blood sample at Day 28 in this group. Proportion of Participants with at least a 4-fold rise in SBA-BR Antibody Titers Table B-5 shows the proportion of participants with a >4-fold rise in Day 28 and Month 6 SBA antibody titers from baseline. Twenty-eight to 56 days after receiving TetraMenD, the majority of participants experienced a > 4-fold rise in the SBA-BR antibody titer for each of the serogroups contained in the vaccine. Table B-5: Percentage and Number of Participants with a >4-Fold Rise in Day 28 and Month 6 SBA-BR Antibody Titers From Baseline (Per-Protocol Population) Test Type Test Date TetraMenD%* Serogroup A SBA Day 28 87.7 (84.9, (558/636) 90.2) 83.8 (80.7, 86.5) (547/653) Month 6 79.1 (75.6, (480/607) 82.2) 56.9 (52.9, 60.8)(354/622) ■; Serogroup C SBA Day 28 73.4 (69.8, (466/635) 76.8) 68.9 (65.2, 72.4) (449/652) Month 6 55.7 (51.6, (338/607) 59.7) 43.7 (39.8, 47.7) (272/622) Serogroup y SBA Day 28 56.6 (52.7, (359/634) 60.5) 45.7 (41.8, 49.6) (298/652) Month 6 57.3 (53.3, (348/607) 61.3) 39.2 ,,., (35.3, 43.2) (243/620) Serogroup W-135 SBA Day 28 91.0 (88.5, (578/635) 93.1) 85.4 (82.5, 88.0) (556/651) 77 Table B-5: Percentage and Number of Participants with a ?4rFold Rise in Day 28 and Month 6 SBA-BR Antibody Titers From Baseline (Per-Protocol Population) Test Type Test Date TetraMenD%* Menomune*o * Month 6 82.7 (79.5, (502/607) 856) 69.5 _iii( (65.7,73.1) (432/622) * %: t n: number of participants with > 4-fold rise from baseline titer. $ N: total number of participants in the used population. Proportion of Participants with Undetectable Titers ( Day 28 SBA-BR Antibody Titers Rise in In both treatment groups and for all vaccine serogroups, most participants with an undetectable (4-fold rise in Day 28 SBA titers. (Table B-6) The proportions of participants with an SBA titer 4-fold rise from baseline to Day 28 ranged from 86.21% to 98.57% in the TetraMenD group; and from 75.00 to 94.64 in the Menomune group. 78 Table B-6: Number and Percentage of Participants with Undetectable Titers ( TetraMenD Menomune® Serogroup %( * ) 95% CI* % 0 95% Clf A 98.57 (275 / 279) (96.37,100.00) 94.64 (265 / 280) ( 91.32,100.00) C 87.87 (297 / 338) (83.91,100.00) 80.05 (293 / 366) ( 75.59,100.00) Y 86.21 (75/ 87) (77.15,100.00) 75.00 (72/ 96) ( 65.12,100i00) W-135 96.00 (384 / 400) (93.59,100.00) 89.53 (359/401). ( 86.11,100.00) *n = The number of participants with titers N = The number of participants with titers Exact 95% confidence interval for the percentage SBA-BR Antibody GMTs and mean fold rises Table B-7 shows the SBA GMTs at baseline and on Day 28 and Month 6 after vaccination and the fold rises in SBA GMTs. Table B-7: SBA-BR Serology Results at Baseline, Day 28, and Month 6 After Vaccination (Per-Protocol Population) TetraMenD Menomune* Test Type Parameter* Bleed Geometri Geomet Nt c Mean (95% CI) Nf ric Mean (95% CI) Serogroup Titer 638 35.44 (29.77, 655 32.72 (27.71, A SBA DayO 42.20) 38.63) Day 28 637 1700.27 (1512.07, 1911.89) 654 892.20 (789.97, 1007.66) Month6 607 1053.65 (912.93, 1216.07) 623 214.97 (179.84, 256.97) Fold rise DayO 638 1.00 ( 1.00, 1.00) 655 1.00 ( 100, 1.00) Day 28 636 35.18 (29.72, 41.65) 653 20.21 (17.43, 23.44) 79 Table B-7: SBA-BR Serology Results at Baseline, Day 28, and Month 6 After Vaccination (Per-Protocol Population) TetraMenD Menomune • Test Type Parameter" Bleed Geometri Geomet Nt c Mean (95% CF) Nt i ricMean (95% CI) Month 607 23.19 (19.20, 622 5.04 ( 4.21, 6 28.00) ;!" Serogroup Titer 638 20.63 ( 17.59, 655 18.69 ( 15.95, CSBA DayO 24.20) 21.90) Day 28 636 353.85 ( 307.95, 406.58) 653 230.71 (197.72, 269.20) ■ Month 6 607 136.92 (116.40, 161.06) 623 65.51 (54.64, 78.55) Fold rise DayO 638 1.00 ( 1.00, 1.00) 655 1.00 ( 1.00, 1.00) Day 28 635 11.86 ( 10.19, 13.81) 652 8.40 ( 723, 9.77) Month 6 607 4.49 ( 3.85, 5.25) 622 2.41 ( 2.05, 2.83) Serogroup Titer 637 118.61 (102.49, 654 117.84 (101.98, YSBA DayO 137.27) 136.18) Day 28 636 636.70 ( 563.06, 719.97) 654 408.10 (362.19, 459.84) Month 6 608 591.77 ( 514.65, 680.43) 622 239.18 (204.91, 279.17) Fold rise DayO 637 1.00 ( 1.00, 1.00) 654 1.00 ( 1.00, 1.00), Day 28 634 4.83 ( 4.25, 5.49) 652 3.14 ( 2.79, 3.52) Month 6 607 4.63 ( 4.00, 5.37) 620 1.85 ( 1.60, 2.14) Serogroup Titer 638 12.09 ( 10.62, 654 12.15 (10.69, W-135 SBA DayO 13.76) 13.80) Day 28 636 749.78 ( 657.37, 855.18) 653 424.75 (371.47, 485.67) Month 6 607 362.25 (311.67, 421.03) 624 136.06 (118.08, 156.78) Fold rise DayO 638 1.00 ( 1.00, 654 1.00 ( 1.00, 1.00) 1.00) Day 28 635 40.24 ( 34.30, 47.21) 651 22.98 (19.73, 26.76) Month 607 19.19 (16.31, 622 7.42 ( 6.33, 6 22.56) 8.69) 80 Table B-7: SBA-BR Serology Results at Baseline, Day 28, and Month 6 After Vaccination (Per-Protocol Population) Test Type Parameter* Bleed TetraMenDGeometriNt c (95% CI) Mean Menomune®GeometNt tic (95% CI) Mean * Titer or fold rise, where fold rise = titer at Day 28/titer at Day 0 tN: total number of participants used in the calculation. EUSA IgG for serogroups A, C, W-135, and Y Table B-8 shows the IgG GMCs at baseline and on Day 28 and Month 6after vaccination and the fold rises in IgG GMCs. Table B-8: IgG Serology Results at Baseline, Day 28, and Month 6 After Vaccination (Per-Protocol Population) Test Type Parame ter Bleed TetraMenD Menomune® Nt Geom etric Mean (95% CI) Nt Geomettic Mean (95% CI) SetogtoupA(IgG)EUSA Titer DayO 115 0.36 ( 0.31, 0.43) 113 0.33 ( 0.28, 0.38) Day 28 115 7.65 ( 6.27, 9.33) 110 6.81 ( 5.51, 8.42) Month S 112 1.70 ( 1-37, 2.11) 109 4.53 ( 3.60, 5.70) Fold rise Day 115 1.00 ( 1.00, 1.00) 113 1.00 ( 1.00, 1.00) Day 28 115 21.00 (16.60, 26.58) 108 21.09 (16.78, 26.50) month 6 112 4.58 ( 3.65,5.75) 107 14.40 ( H-22, 18.49) SetogtoupC(IgG)EUSA Titer DayO 115 0.23 ( 0.20, 0.25) 113 0.25 ( 0.22, 0.29) Day 28 115 1.24 ( 1.03, 1.50) 110 7.62 ( 6.33, 9.19) Month 6 111 0.36 ( 0.31, 0.43) 109 3.49 ( 2.82, 4.32) Fold rise DayO 115 1.00 ( 1.00, 1.00) 113 1.00 ( 1.00, 1.00) Day 28 115 5.50 ( 4.58, 6.62) 109 30.18 (24.26,37.55) Month 6 111 1.60 ( 1-36, 1.89) 107 14.42 ( 1.1.46, 18.15) 81 Table B-8: IgG Serology Results at Baseline, Day 28, and Month 6 After Vaccination (Per-Protocol Population) Test Type Parameter* Bleed TetraMeaD Menomune* Nt GeometricMean (95% CI) Nt Geometrk Mean (95% CI) SerogroupY(IgG)ELISA Titer DayO 115 0.38 ( 0.34, 0.43) 114 0.34 ( 0.31, 0.38) Day 28 115 1.54 ( 1.26, 1.88) 110 4.15 ( 3.30, 5.22) Month 6 112 0.76 ( 0.65, 0.89) 109 ; 2.90 ( 2.25, 3.73) Fold rise DayO 115 1.00 ( 1.00, 1.00) 114 1.00 ( 1.00, 1.00) Day 28 115 4.04 ( 3.30, 4.93) 109 12.43 ( 9.85, 15.68) Month 6 112 1.98 ( 1.68, 2.32) 108 8.72 ( 6.79, 1121) Serogroup W-135(tG)ELISA Titer DayO 115 0.25 ( 0.22, 0.28) 113 0.22 ( 0.19, 0.25) Day 28 115 0.90 ( 0.72, 1.12) 110 2.53 ( 3.11) Month 6 112 0.55 ( 0.47, 0.65) 109 1.88 ( 1-53, 2.31) Fold rise DayO 115 1.00 ( 1.00, 1.00) 113 1.00 ( 1.00, 1.00) Day 28 115 3.60 ( 2.90, 4.47) 108 11.67 ( 9.34, 14.58) Month 6 112 2.18 ( 1-84, 2.58) 107 8.70 ( 6.96, 10.87) Titer or fold rise, where fold rise = titer at Day 28/titer at Day 01N: total number of participants used in the calculation. Twenty-eight to 56 days after receiving the study vaccination, TetraMenD, the majority of participants experience a 4-fold rise in the SBA-BR antibody titer for each of the serogroups contained in the vaccine. Overall, 77% of TetraMenD recipients experience a 4-fold rise in antibody titer across all serogroups. Higher pre-vaccination antibody levels are observed for serogroup Y than for C or W-135. This may be related to the feet that natural exposure to serogroup Y at this age may be more common than previously thought Higher circulating antibody levels reflect recent natural exposure and may reduce the proportion of vaccine recipients exhibiting 4-fold or higher antibody responses. This clearly 82 post-vaccination SBA-BR titer of > 1:32 and 90.5% achieved a titer ? 1:128. A subset of sera from this clinical study is also used to evaluate the correlation between the SBA assay using baby rabbit complement and human complement and the results are provided in a subsequent Study. Total IgG responses are significantly higher for serogroups C, Y, and W-135 in the Menomune® group than in the group receiving TetraMenD. However, the post-vaccination SBA GMT levels for serogroups A, C, Y, and W-135, are significantly higher in the TetraMenD group. Table B-9 provides a comparison of GMC versus GMT titers by serogroup. Table B-9 Comparison of IgG GMC and SBA GMTs Titers by Serogroup Serogroup Day 28 Results: IgG GMC SBA GMT A TetraMenD 7.65 1700.3 Menomune® 6.81 8922 C TetraMenD 1.24 353.9 Menomune 7.62 230.7 Y TetraMenD 1.54 636.7 Menomune® 4.15 408.1 W-135 TetraMenD 0.90 749.8 Menomune® 2.53 424.8 The observation that the lower levels of IgG produced by the conjugate generated a higher level of bactericidal activity than the polysaccharide vaccine strongly suggests that the quality and affinity of the antibody response to the conjugate vaccine is superior to that generated by conjugated polysaccharide vaccine. High affinity antibody is associated with functional activity and memory response. This effect has also been observed in several published studies. These data demonstrate that TetraMenD is highly immunogenic in children aged 2 to 10 years, the observed GMTs in the TetraMenD group are superior to those observed in the Menomune group for each of the four serogroups, and the titers achieved are predictive of protection. Finally, it appears that TetraMenD generates higher affinity antibody responses for each serogroup contained in the vaccine. Safety is monitored at 4 specific time points during the trial: Immediate reactions (within 30 minutes of vaccination), solicited local and systemic reactions within the first 7 days 84 post-vaccination, all adverse events in the 28-day period after vaccination and continuing AEs (from Days 0-28) and serious adverse events from Day 0 to 6 months post-vaccination are reported. For all participants, most local solicited reactions for both treatment groups are reported as mild and resolved within 3 days of vaccination. The frequency of local reactions is similar for each treatment group. In the group receiving TetraMenD 58.8% reported at least one local reaction while the group receiving Menomune® 58.3% reported the same. In addition, experience with the monovalent C CRM197 conjugate vaccine given intramuscularly to adolescents shows that the rate of local reactions is very similar that observed for TetraMenD in this study. The majority of reported AEs are not serious, reversible, and unrelated to vaccination. There are no reports in this study of new onset bronchial asthma, diabetes ;mellitus, or 15 autoimmune disease. Example 12 Study C One Month Study in Children Aged 11 to 18 Study C is a randomized, active-controlled study of healthy children aged 11 to 18 years as of DO of a single dose of TetraMenD versus a single dose of Menomune®. Blood serum is drawn on DO, prior to vaccination and D28 and analyzed, and a subset of sera from patients is further evaluated as described in the results. For all participants, most local solicited reactions for both treatment groups are reported as mild and resolved within 2 days of vaccination. The frequency of local: reactions is more common in the group receiving TetraMenD (72.4%) than in the group receiving Menomune (34.7%). This result is probably due to the nature of the conjugate vaccine (diphtheria carrier protein) rather than the route of administration (intramuscular). The results of this Study are summarized in the following Tables. Table C-1 shows the frequency distribution of baseline and Day 28 SBA-BR antibody titers for each serogroup. 85 Table C-1: Distribution of SBA-BR Antibody Titers at Day 0 and Day 28 After Vaccination (Per-Protocol Population) SBA-BR Titers — Test Type Test Date Group (N)* SBA(A) DayO TetraMenD(425) 81 (19.1) 19 (4-5) 4 (0.9) 9 (2.1) 33 (7.8) 76 86 51 (17.9) (20.2) (12.0) MO® (423) 93 (22.0) 12 (2.8) 10 (2-4) 13 (3.1) ■ Ki38 (9.0) 72 72 56 (17.0) (17.0) (13.2) Day28 TetraMen D (423) # - - - 1 (0.2) " - 1 (0.2) 15 (3.5) Menomun e® (423) - - - - - 8 (1.9) 12 (2.8) 19(4.5) SBA(C) DayO TetraMen D 157 (36.9) 37 (8.7) 18 (4.2) 24 (5.6) 36 (8.5) 40 (9.4) 39 (9.2) 35 (8.2) Mee® (423) 152 (35.9) 35 (8.3) 15 (3.5) 19(4.5) 40 (9.5) 46 (10.9) 42 (9.9) 25 (5.9) Day28 TetraMen (4D23) 1 (0.2) 1 (0.2) 1 (0.2) „.,2 (0.5) 17 (4-0) 33 (7.8) 58 (13.7) Menomun (423^ 1 1 1 4 26 47 56 86 Table C-1: Distribution of SBA-BR Antibody Titers at Day 0 and Day 28 After Vaccination (Per-Protocol Population) SBA-BR Titers TestType TestDate Group (N)* SBA00 DayO TetraMenD(425) 61(14.4) 6(1.4) 1 (0.2) 22 (5.2) 64 (15.1) 94 (22.1) 101 (23.8) 50 (11.8) MO® (423) 47 (11.1) 3 (0.7) 7 (1.7) 27 (6.4) 74 (17.5) 94 (22.2) 85 (20.1) 51 (12.1) Day28 TetraMenD(423) - - 1 (0.2) 1 (0.2) 23 : (5.4) 53 (12.5) 71 (16.8) Menomune® . (423) 1 (0.2) - - - 2 (6-5) 11 (2.6) 59 (13.9) 81 (19.1) SBA M- DayO TetraMen D 165 (38.8) 37 (8.7) 28 (6.6) 36 (8.5) 60 (14.1) 56 (13.2) 22 (5.2) 15(3.5) (423) 139 (32.9) 52 (12.3) 25 (5.9) 34 (8.0) 67 (15.8) 43 (10.2) 46 (10.9) 11 (2.6) Day28 TetraMenn (423) 4 (0.9) 1 (0.2) (0.2) 19 (4-5) 34 (8.0) 63 (14.9) Menomun (423) 1 (0.2) 1 (0.2) 1 (0.2) 2 (0.5) 12; (2.8) 21 51 (5.0) (12.1) 87 Table C-1: Distribntion of SBA-BR Antibody Titers at Day 0 and Day 28 After Vaccination (Per-Protocol Population) SBA-BR Titers 1024 to >65536 Test Type Test Date Group (IN)* 1024n(% 2048n(% 4096n(% 8192nj% 16384n(% 32768n(%) 65536 n (%) >6553n (%) SBA(A) DayO TetraMen D 32 (7.5) 29 (6.8) 2 (0.5) 1 (0.2) 2 (0.5) Me 6® un (423) 38 (9.0) 14 (3.3} 2 (0.5) 2 (0.5) 1 (0.2) - - - Day28 Te L/ en(423) 36 (8.5) 66 (15.6) 90 (21.3) 108 (25.5) (64.9 37 (8.7) 4 2 (0.9) (0.5) Me 6Qy un(423) 46 (10.9) 100 (23.6) 108 (25.5) 76 (18.0) i~20 11 (2.6) - SBA(C) DayO TetraMen 20 (4.7) 13 (3.1) 4 (0.9) 2 (0.5) e®(423) 23 (5.4) 22 (5.2) 2 (0.5) 1 (0.2) 1(0.2) - - - Dav28 TetraMen (423) 66 (15.6) 82 (19.4) 66 (15.6) 45no.6) 24 (5.7) 21 (5.0) 4 (0.9) 2 (0.5) Menomun (423) 70 (16.51 64ns.n 55 41 (9.71 35 (8.31 19 3(0.71 88 Table C-1: Distribution of SBA-BR Antibody Titers at Day 0 and Day 28 After Vaccination (Per-Protocol Population) SBA-BR Titers 1024 to >65536 Test Type Test Date Group (N)* 1024 n(%) 2048 n(%) 4096n(%) 8192n(%) 16384n(%.)"" 32768n(%) 65536n(%) >65530n(/o) SBA DayO TetraMenD(425) 13 (3.1) 6 (1.4) 2 (0.5) 2 (0.5) 2 (0.5) 1 (0.2) - - Mee® un 24 (5.7) 6 (1.4) 2 (0.5) 1 (0.2) 1 (0.2) 1 (0-2) - - Day28 TetraMenD(423) 77 (18.2) SO (18.9) 52 (12.3) 41 (9.7) 16 (3.8) 7 (1.7) 1 (0.2) - Menomun. e® (423) 90 (21.3) 74 (17.5) 53 (12.5) 35 (8.3) 11 (2.6) 6 (1.4) - SBA(w-135) DayO TetraMen D 4 (0.9) 2 (0.5) - - - - - - Menomun e 4 (0.9) 1 (0.2) 1 (0-2) - - - - - Day28 TetrD en (423) 90 (21.3) 88 (20.8) 64 (15.1) 36 (8.5) 16 (3.8) 6 (i-4) 1 (0.2) - Meno® un (423) 103 T24.3) 114 (27.0) 67 (15.81 42 (9.9) 6 (1;4) 2 (0.5) C-2 summarizes GMT Age and Serogroup for TetraMenD Table levels by Subject Table C-2 of GMT by Subject Age and Serogroup for TetraMenD Age(inYear) Blood Day No. of Subjects SerogroupAGMT Serogroup CGMT SerogroupWGMT SerogroupY-135GMT 11 DayO 45 101.59 37.33 21.77 91-21 Day 28 45 4705.07 1372.15 1482.00 1024.00 12 DayO 54 10424 42.99 14.63 72,77 Day 28 53 5049.37 2157.99 1245.94 1198.00 13 DayO 65 145.47 32.34 20.23 128.00 89 Day 28 65 7363.39 1880.53 2206.73 1782.89 14 DayO 67 85.50 31.67 24.71 107.36 Day 28 67 5124.87 2006.06 1753.62 1159.35 15 DayO 70 129.27 42.22 27.31 126.74 Day 28 68 4870.99 2090.18 1193.17 1193.17 16 DayO 69 103.66 21.41 22.74 129.29 Day 28 69 7189.09 2357.27 1455.45 ,., 2068.68 17 DayO 69 85.64 38.73 13.90 72.93 Day 28 67 4269.06 1665.21 841.27 904.45 18 DayO 1 4 8 16 64 Day 28 1 8192.00 256.00 512.00 8192.00 Table C-3 shows the numbers and percentages of participants with a >_4-fold rise in SBA-BR titer from baseline to Day 28 for the serogroups A, C, Y, and W-13,5. For each serogroup, these percentages are higher in the TetraMenD group than in the Menomune* group. Table C-3: Numbers and Percentages of participants with a >_4-fold rise in SBA-BR titer from Baseline to Day 28 4-fold risein SBA titer forserogroup TetraMenDn/N P Proportion Menomune"1" PmProportion— .M.tDifference-pt) Upper bound of the one sided 95%if Difference A 392/423 0.9267 391/423 0.9243 NA NA C 388/423 0.9173 375/423 0.8865 -0.0307 0.0029 Y 346/423 0.8180 339/423 0.8014 -0.0165 0.0278 W-135 409/423 0.9669 403/423 0.9527 -0.0141" 0.0080 Frequency of SBA-BR Antibody Titers > 32 The proportion of participants with SBA antibody titers > 32 at Day 28 after vaccination is 10 summarized in Table C-4. 90 Table C-4: Percentage and Number of Participants with an SBA Antibody Titer > 32 at Day 28 Post-Vaccination (Per-Protocol Population) TetraMenD Menomune® %* 95% Q for (n«/N*) the percentage %* ,,, 95%Q for (nt /N*) the percentage Serogtoup A 100.00 (423/423) (99.13, 100.00) 100.00 (423/423) (99.13, 100.00) Serogtoup C 99.53(421/423) (98.30, 100.00) 99.53(421/423) (98.30, 100.00) Serogtoup Y 99.76(422/423) (98.69, 100.00) 99.76(422/423) (98.69, 100.00) Serogtoup W-135 (498-423) (97.26, 100.00) (429-423, (98.30, 100.00) %: t n: number of participants with titer>32 at Day 28 post-vaccination. N: total number of partidpan with valid blood sample at Day 28 in this group. ts* Frequency of SBA-BR Antibody Titers >_ 128 The proportion of participants with SBA antibody titers >_ 128 at Day 28 after vaccination is summarized in Table C-5. 91 Table C-5: Percentage and Number of Participants with an SBA Antibody Titer > 128 at Day 28 Post-Vaccination (Per-Protocol Population) , ,,.,, TetraMenD Menomane %* (nVN*) 95% Q for the percentage %* (nVN*) 95% CI for the percentage SerogroupA 99.76(422/423) (98.69,100.00) 100.00 (423/423) (99.13,100.00) SerogroupC (418/423) *JE(97.26,100.00) 835 (416/423) (96.62,100.00) SerogroupY 9.53 (421/423) (98.30,100.00) 9929 (420/423) (97i94,100.00) SerogroupW-135 98.58 (417/423) (96.94,100.00) 98.82 (418/423) (9726,100.00) *%:n/N expressed as a percentage. t n: number of participants with titer>128 at Day 28 post-vaccination. N: total number of participants with valid blood sample at Day 28 in this group. Percentage of Participants with > 4-fold Rise in SBA-BR Antibody Titers Table C-6 shows the proportion of participants with a >4-fold rise in Day 28 SBA antibody titers from baseline. 92 Table C-6: Percentage and Number of Participants with a >4-Fold Rise.in Day 28 SBA Antibody Titers From Baseline Test Type TetraMenD Menomane* %*( (95% a) %* (nVN*) (95% CI) Serogroup A SBA 92.7 (392/423) (89.8,95.0) 92.4 (391/423) (89.5,94.8) Serogroup C SBA (3 8/423) (88.7,94.2) (375s87/423) (852,91.5) Serogroup Y SBA 81.8 (346/423) (77.8,85.4) 80.1 (339/423) (76.0,83.8) Serogroup W-135 SBA 9.7 (409 (94.5,982) 9.3 (4035423) (92.8,97.1) %: n/N expressed as a percentage.. t n: number of participants with > 4-fold rise from baseline titer. N: total number of participants in the used population. Percentage of Participants with Undetectable Titers (4-Fold Rise in Day 28 SBA-BR Antibody Titers In both treatment groups and for all vaccine serogroups, most participants with an undetectable (4-fold rise in Day 28 SBA titers. The proportions of participants with an SBA titer 4-fold rise from baseline to Day 28 range from 98.17% to 100.0% (Table C-7). Table C-7: Number and Percentage of Participants with Undetectable Titers (4-Fold Rise in Day 28 SBA-BR Antibody Titers. TetraMenD Menomune® Serogroup Percent n/N* 95% a* Percent n/N 95%CIt A 100.00 81/81 (95.55,100.00) 100.00 93/93 (96.11,100.00) C 98.71 153/155 (95.42,100.00) 99.34 151/152 (96.39,100.00) Y 98.17 161/164 (94.75,100.00) 9928 138/139 (96.06,100.00) W-135 98.36 60/61 (91.20,100.00) 100.00 47/47 (92.45,100.00) n = The number of participants with titers 32 at Day 28 within each serogroup N = The number of participants with titers 93 SBA-BR Antibody GMTs and mean fold rises Table C-8 shows the SBA GMTs at baseline and on Day 28 after vaccination and the fold rises in SBA GMTs. Table C-8: SBA Serology Results at Baseline and at Day 28 After Vaccination (Per-Protocol Population) Test Type Parameter Bleed TetraMenD Menomune* Nt Geometric Mean (95% CI) Nt Geometric Mean CI) Serogroup A SBA Titer DayO 425 10628 (87.60, 128.95) 423 88.6^7 (73.05, 107.64) Day 28 423 548321 (4920.12. 6110.74) 423,, 3245.6t 7 (2909.97, 3260.11) Fold rise Day 28 423 44.92 54.57) 423 31.43 (3 1.0) Serogroup CSBA Titer DayO 425 33.71 (27.54, 41.28) 423 37.39 (30.40, 45.98) Day 28 423 1924.36 (1662.08. 2228.03) 423 1638.87 (1405.55. 1910.93) Fold rise Day 28 423 43.83 52 78) 423 34.17 (41..24) Serogroup YSBA Titer DayO 425 103.21 (87.80,121.32) 423 111.91 (96.03, 130.41) Day 28 423 1322.26 (1161.85, 1504.82) 423 1228.21 (1088.20. 1386.37) Fold rise Day 28 423 11.62 13.60) 423 10.16 18.79) SerogroupW-135SBA Titer DayO 425 20.70 (1730, 24.22) 423 23.90i (20.40, 28.02) Day 28 423 1407.22 (1232.07 1607.27^ 423 1544.9 9 (1383.63, \125.\6 Fold rise Day 28 423 51.98 .36, * Titer or fold rise, where fold rise = titer at Day 28Aiter at Day 0 N: total number of participants used in the calculation. ELISA IgG for serogroups A, C, W-135, and Y Table C-9 shows the IgG GMCs (in μglmL) at baseline and on Day 28 after vaccination and the fold rises in IgG GMCs. 94 Table C-9: IgG Serology Results at Baseline and at Day 28 After Vaccination (Per-Protocol Population) Test Type Parameter* Bleed TetraMenD Menomune* M GeometricMean (itg/mL) f95% CD Nr Geometric Mean (g/mL) (95% C n Serogroup A (IgG)ELISA Titer DayO 82 0.84 (0.61, 79 0.62 (0.45, 0841 28 Day 82 18.09 (13.56, 24.12) 79 11.61 (8.81, 15.29) Fold rise Day 28 82 21.49 28 24) 79: 18.87 25.00) Seroeroup C (IgG) ELISA Titer Day 0 82 0.27 (023, 0.31) 79; 0.30 (0.24, 0.37) Dav28 82 5.54 (3.85, 7.97) 79 8.08 (5.37, 12.18) Fold rise Day 28 82 20.78 (14.74, 29.28-> 79 26.97 (18.93, 38.4n Seroeroup Y (IgG) ELISA Titer DayO 82 0.41 (0.32, 0.53) 79, 0.39 (0.30, 0.50) Day 28 82 4.41 (2.74, 7.08) 79! 9.17 (6.58, 12.78) Fold rise Day 28 82 10.81 (7.32, 15.95) 79 23.55 (16.93, 32.75) Gornniviii r»W-135 (IgG) ELISA titer DayO 82 0.24 (0.20, 0.291 79 0.24 (0.19, 0.30) Day 28 82 2.95 (2.02, 79, 4.93 (3.47, 7 CUU Fold rise Day 28 82 12.26 18 78, 79 20.40 1 A. 28.46) * Titer or fold rise, where fold rise = titer at Day 28/titer at Day 0 tN: total number of participants used in the calculation. ELISA IgM for serogroups A, C, Y, and W-135 Table C-10 shows the IgM GMCs at baseline and on Day 28 after vaccination and the fold rises in IgM GMCs. Table C-10: IgM Serology Results at Baseline and at Day 28 After Vaccination (Per-Protocol Population) Test Type Parameter* Bleed TetraMenD Menomune* Nt Geometric Mean (95% CI) Nt Geometric Mean (95% Cn Serogroup A (IgM) ELISA Titer DayO 81 1.66 (1.34, 2.06) 79 1.42 0.15, 1.75) Day 28 80 17.80 (14.67, 21.59) 79 12.00 (9.67, 14.89) 95 Table C-10 shows the IgM GMGs at baseline and on Day 28 after vaccination and the fold rises in IgM GMCs. Table C-10: IgM Serology Results at Baseline and at Day 28 After Vaccination (Per-Protocol Population) j* Test Type Parameter* Bleed TetraMenD Menomune" KH GeometricMean Kit GeometricMean Fold rise Day 28 79 11.22 14.73) 79 8.47 10.°16) SeroerouD C (IgM)ELISA Titer DayO 82 0.19 (0.14, 0.241 79 0.16 (0.12, 0.221 Day 28 80 1.55 (1.20. " 2.00) " 79 1.71 (1.39. 2.10) Fold rise Day 28 80 8.42 I1.I8) 79 10.60 13.97) SeroerouD Y (IgM) ELISA Titer DayO 82 0.37 (0.29, ft 461 79 0.40 (0.32, nsni Day 28 80 3.47 (2.81. 4.27) 79 3.45 (2.85. 4.17) Fold rise Day 28 80 9.47 12.05) 79 8.65 11.03) Serogroup W-135 flaMI ELISA Titer DayO 82 0.17 (0.15, (1201 79 0.18 (0.16. 0 211 n»v2ft 82 1.92 79 1.68 (1 aa Fold rise Day 28 82 11.01 13.°39) 79 9.16 V.61- * Titer or fold rise, where fold rise = titer at Day 28/titer at Day 01N: total number of participants used in the calculation. Twenty-eight to 56 days after receiving the study vaccination, TetraMenD, the majority of participants experience a 4-fold rise in the SBA-BR antibody titer for each of the serogroups contained in the vaccine. Overall, 90.7% of TetraMenD recipients experience a 4-fold rise in antibody titer across all serogroups. Higher pre-vaccination antibody levels are observed for serogroup Y than for C or W-135. This may be related to the fact that serogroup Y is currently the most common serogroup associated with invasive meningococcal disease in this age group in the U.S. and that natural exposure to this serogroup may be more common. Higher circulating antibody levels reflect recent natural exposure and may reduce the proportion of vaccine recipients exhibiting 4-fold or higher antibody responses. This appears to be the case for serogroup Y responses when compared to other serogroups. The 4-fold rise for serogroup Y is 81.8% compared with 91.7% for serogroup C and 96.7% for serogroup W-135. High pre-vaccination antibody levels are also 96 observed for serogroup A. This may be the result of intermittent exposure over a prolonged time to several naturally occurring cross-reacting antigens. To further evaluate the impact of pre-existing titers and to investigate the rate of seroconversion (as defined by the proportion of vaccine recipients who achieve a 4-fold rise in antibody titer when the pre-vaccination titer for any serogroup is ...Ht serogroups contained in the vaccine. A titer of 98.1% for serogroup W-135, and 98.3% for serogroup Y after vaccination with TetraMenD. .HI As previously discussed in another Study, Goldschneider proposed that a minimum titer of > 1:4 using an SBA assay with a human complement source correlated with protection from invasive disease against Serogroup C based on observations in military recruits. However, because of the need for standardization of the assay and the lack of a reliable source of human complement, baby rabbit complement is suggested as an alternative source. Meningococci appear to be more sensitive to the baby rabbit complement than human complement, resulting in higher measured antibody titers. Several authors have suggested that titers 1:128 using the rabbit complement assay are predictive of protection while titers of 1:128. The results for subjects who received the TetraMenD vaccine with SBA-BR titers 1:128 for each serogroup is presented in the Tables. When these criteria are applied to each of the serogroups contained in the, vaccine, overall, 99.2% of participants who received TetraMenD achieved a post-vaccination SBA-BR titer of 1:128. 97 IgG and IgM responses are evaluated in a subset of participants using a standard ELISA assay. Post-vaccination, the mean level of IgG antibody in the TetraMenD) recipients is > 2 tg for each serogroup. IgM responses are very similar for each serogroup in both treatment anus. The IgG responses are generally higher for serogroups C, Y, and W-135 in the Menomune* group than in the group receiving TetraMenD. The post-vaccination SBA GMT levels for serogroups C, Y, and W-135, however, are very similar in each treatment group, Table C-l 1. Table C-ll: Relative Contribution of IgG and IgM to Total Bactericidal Activity Serogroup Day 28 Results: IgG CMC* IgM CMC SBA OUT A TetraMenD 18.09 17.80 5483.21 Menomune" 11.61 12.00 3245.67 C TetraMenD 5.54 1.55 1924.3 6 Menamune" 8.08 1.71 1638.87 Y TetraMenD 4.41 3.47 1322.26 Menomune 9.17 3.45 1228.27 W-135 TetraMenD 2.95 1.92 1407.22 Menomune" 4.93 1.68 1544.99 i * GMC units are Ug/mL The observation that the lower levels of IgG produced by the conjugate generated a similar level of bactericidal activity as the polysaccharide vaccine strongly suggests that the quality and affinity of the antibody response to the conjugate vaccine is superior to that generated by the polysaccharide. It is the high affinity antibody that is associated with functional activity and memory response. This effect has also been observed in several published studies. These data demonstrate that TetraMenD is highly immunogenic in the adolescent population. The GMTs are essentially equivalent for each of the four serogroups for both vaccines, and the titers achieved are predictive of protection, and it appears that TetraMenD generates higher affinity antibody responses for each serogroup contained in the vaccine. 98 Study D Study D is a randomized, active-controlled study of healthy adults aged 1$ to 55 years as of DO of a single dose of TetraMenD versus a single dose of Menomune®, Blood serum is drawn on DO, prior to vaccination and D28 and analyzed. Generally, the safety profile of TetraMenD is comparable to Menomune, specifically, the percentages reported for Solicited Local Reactions (Days 0-7), Solicited: Systemic Reactions (Days 0-) Unsolicited Adverse Events (Days 0-28) Unsolicited Significant Adverse Events and SAEs (Day 29-Month 6) Serious Adverse Events (Day 0-Month 6),are all within 2-3% of the percentages reported for Menomune. The results of the Study are provided in the following Tables. Distribution of SBA-BR Antibody Titers Table D-1 shows the frequency distribution of baseline and Day 28 SBA-BR antibody titers 15 for each serogroup. 99 Table D-2 provides a summary of the Geometric Mean Ther (GMT) by Subject Age and Serogroup forTetraMenD. Table D-2 Summary of GMT by Subject Age and Serogroup for TetraMenD Age Blood No. of Serogroup Serogroup Serogroup Serogroup (in Day Subjects A CGMT W Y-135 Year) GMT GMT GMT 18 DayO 127 238.47 45.63 *2.04 111.67 Day 28 122 5170.42 2690.10 1613.23 2556.00 19. DayO 132 224.51 40.96 37.66 244.18 Day 28 127 4421.24 2425.55 1786.78 ■•""" 2492.65 20 DayO 107 193.76 69.62 41.73 108.16 Day 28 103 5080.24 3193.18 1766.17 1966.95 21 DayO 106 239.80 57.27 32.42 12227 Day 28 105 3911.03 2447.58 1521.66. 1725.00 22 DayO 84 371,11 47.95 34.18 175.14 Day 2* 82 4649.72 3151.78 1729.45 3151.78 23 DayO 81 219.45 54.40 50.80 18025 Day 28 80 4664.48 3788.73 1620.81 1961.17 24 DayO 66 223.33 71.84 42.49 124.03 Day 28 64 3922.34 3057.48 1479.87 156221 25 DayO 62 289.50 48.94 29.26 148.02 Day 28 59 4771.87 3685.02 2121.47 1563.07 26 DayO 29 131.10 37.83 17.19 73,87 Day 28 26 4936.36 4320.32 1170.01 2673.69 27 DayO 20 315.17 45.25 28.84 445.72 Day 28 20 5042.77 5595.30 803.41 2702.35 28 DayO 33 593.10 72.60 55.25 157.92 Day 28 33 6640.01 4948.33 1558.63 2091.47 29 DayO 26 270.02 29.54 28.76 51/71 Day 28 26 4936.36 2534.86 1201.62 2278.46 30 DayO 19 229.46 68.84 25.71 99.15 Day 28 19 5287.69 5687.92 1645.39 1529.61 31 DayO 17 138.88 52.20 27.18 226.53 Day 28 17 2314.48 3340.58 1111.00,. 1966.18 32 DayO 24 362.04 58.69 64.00 50.80 Day 28 24 4732.32 354524 1448.15 1933.05 33 DayO 22 329.39 10934 68.16 164.69 Day 28 22 2989.02 3499.00 1317.54 1749.50 34 DayO 16 534-67 51.54 41.50 112.40 Day 28 15 3734.42 4096.00 741.00 1415.08 35 DayO 17 369.50 156.95 19.62 48.11 Day 28 16 4096.00 6888.62 824.57 , 1649.14 36 DayO 17 192.44 69.44 20.43 156.95 Day 28 17 3078.98 7864.70 136224 2410.80 102 37 DayO 20 238.86 78.79 20.39 73.52 Day 28 19 1835.69 4406.03 637.28 1474.81 38 DayO 24 203.19 90.51 15.54 78.34 Day 28 24 3158.45 4216.02 558.34 - 1824.56 39 DayO 18 376.25 61.58 33.26 143:68 Day 28 18 4778.10 4096.00 1824.56 1970.63 40 DayO 25 249.00 71.51 25.63 86.82 Day 28 25 3983.99 3769.09 916.51 1112.82 41 DayO 26 242.71 60.68 23.24 131I.46 Day 28 26 3681.69 2403.25 1201.62 1336.84 42 DayO 24 128.00 71.84 25.40 32.94 Day 28 24 2435.50 2169.78 542.45 : 574.70 43 DayO 23 144.40 51.83 33.99 72.70 Day 28 23 2453.92 1815.42 1120.89 1515.12 44 DayO 27 198.04 101.59 47.03 99.02 Day 28 27 2647.42 3335.54 1194.53 998.05 45 DayO 23 158.06 53.41 31.05 79^03 Day 28 23 2241.79 2686.11 453.85 1561.48 46 DayO 28 204.87 55.17 21.53 68.93 Day 28 28 2205.89 1680.05 927.46 ,.,. 1217.75 47 DayO 20 187.40 81.57 32.00 87.43 Day 28 20 2352.53 4544.80 652.58 1351.18 48 DayO 32 94.52 38.05 25.22 139.58 Day 28 32 3158.45 2435.50 939.01 1299.51 49 DayO 19 114.73 33.19 24.79 137.69 Day 28 19 2048.00 4096.00 951.95 1586.44 50 DayO 16 145.76 94.52 34.90 98.70 Day 28 16 3922.34 2048.00 693.38 .,,, 1024.00 51 DayO 15 73.52 29.18 27.86 67.03 Day 28 15 1702.38 2702.35 280.79 370.50 52 DayO 12 135.61 90.51 11.99 95.89 Day 28 12 2169.78 3251.00 542.45 542.45 53 DayO 11 272.65 128.00 49.74 105.95 Day 28 11 1922.93 1922.93 423.81 350-81 54 DayO 10 84.45 90.51 9.19 238.86 Day 28 10 2702.35 3104.19 222.86 .... 1176.27 55 DayO 6 71.84 22.63 57.02 50.80 Day 28 6 812.75 3649.12 512.00 724.08 Table D-3 shows the numbers and percentages of participants with a >_4-fold rise in SBA-BR titer from baseline to Day 28 for the serogroups A, C, Y, and W-135. The numbers and percentages for the serogroups A, 1028/1278 (80.4%); C, 1131/1278 (88.5%); Y, 941/1278 (73.6%); and W-135, 1142/1278 (89.4%) in the TetraMenD group are comparable to those in the Menormine® group, with serogroups A, 929/1099 (84.5%); C, 985/1099 (89.6%); Y, 872/1099 (79.3%); and W-135,1036/1099 (94.3%). 103 Table D-3: Number and Percentage of participants with a 4-Fold Rise from Baseline in SBA-BR Titer by Serogroup -fold rise in SBA-BRtiter for Serogroups TetraMenD Menomune % Difference"ppMcnomuiK—i®. : PTetraMe„D) Upper onesided 97.5% Confidence limit of the Difference n/N- TetraMenD n/N rMenomune*E A 1028/1278 80.4 929/1099 84.5 4.1 7.1 C 1131/1278 88.5 985/1099 89.6 " 1.1 3.6 Y 941/1278 73.6 872/1099 79.3 5.7: 9.1 W-135 1142/1278 89.4 1036/1099 94.3 4.9 7.1 * Testing the null hypothesis Ho: PMenomune - PTetiaMenD ?0.10 VerSUS Ha: PMenomune -PTetraMenD t n/N: n = number of participants with a >_4-fold rise from baseline titer / N = total number of participants in the per-protocol population. $ PTe CD: percentages of participants with a >_4-fold rise from baseline in SBA-BR post-vaccination titer from the TetraMenD group. § PMenomune®: percentages of participants with a >_4-fold rise from baseline in SBA-BR post-vaccination titer from the Menomune® group. Frequency of SBA-BR Antibody Titers > 32 The proportion of participants with SBA-BR antibody titers > 32 at Day 28 after vaccination is summarized in Table D-4. 104 Table D-4: Percentage and Number of Participants with an SBA Antibody Titer > 32 at Day 28 Post-Vaccination (Per-protocol _ _ ~ . .lit Population) Tetra MeanD Menomune® %*(n/N>t 95% CI for the percentageOf %* fn/NV 95% CI for the percentage Serogroup A 100.0 (1278/1278) (99.77%, 100.00%) 99.9 (1098/1099) (99.49%, 100.00%) Serogroup C 99.5 (1272/1278) (98.98%, 99.83%) 98.9 (1087/1099) (98.10%, 99.43%) Serogroup Y 97.8 (1250/1278) (96.85%, 98.54%) 98.9 (1087/1099) (98.10%, 99.43%) Serogroup W-135 98.7 (1261/1278) (97.88%, 99.22%) 99.2 (1090/1099) (98.45%, 99.62%) *%: = n/N tn: number of participants with a titer > 32 at Day 28 post-vaccination / N: total number of with a valid partici blood pan sample at Day 28 in this group. Frequency of SBA-BR Antibody Titers > 128 The proportion of participants with SBA-BR antibody titers > 128 at Day 28 after vaccination is summarized in Table D-5. 105 Table D-5: Percentage and Number of Participants with an SBA Antibody Titer 128 at Day 28 Post-Vaccination (Per-protocol Population) TetraMenD Menomune %ft/* A^AS /IT *(n/N)" the percentage % 95% CI for (n/N)" the percentage Serogroup A 99.8 (1276/1278) 99(99.4 (99.44%,no , - 99.9 (1098/1099) (99.49%, 100.00%) Serogroup C 98.7 (1262/1278) 99(97.970%, .28 /o) 98.5 ,.„ (1082/1099) (97.53%, 99.10%) Y Serogroup 96.9 (1239/1278) 97(95.85o%, 98.5 (1082/1099) (97.53%, 99.10%) Serogroup W-135 97.1 (1241/1278) (96.03%, 97.95%) 98.5 (1082/1099) (97.53%, 99.10%) *%: t n: number of participants with a titer 128 at Day 28 post-vaccination. N: total number of participants with a valid blood sample at Day 28 in this group. Table D-6 Analysis of Treatment Effect on GMTs Adjusted by Baseline Covariate: Response of Titer Difference from Day 0 to Day 28 (Per-protocol Population)* Serogroup Baseline GMT EstimatE ofBaselineGMTEffect Difference ofTreatmentEffect(Menomune®=TetraMenD) Anti-Log ofTreatmentEffect*(Menomune®-TetraMenD): 95% CI forAnti-Log ofTreatmenteffect ®(Menomune -TetraMenD) SBA Serogroup A TetraMenD 223.6 -0.850 0.096 1.069 (0.973,1.175) Menomune 203.9 SBA Serogroup C TetraMenD 57.2 -0.772 0.130 1.094 (0.965,1.240) Menomune 51.8 , 106 SBA Serogroup Y TetraMenD 122.9 -0.743 0.469469 1.384 (1.225,1.563) Meriomune 127.4 ■ !"" SBASerogroup W-135 TetraMenD 33.2 -0.766 0.576 1.491 (1.334,1.666) Menomune 31.0 Anti-Log of treatment effectis calculated 2 to the treatment effect TetraMeriD) power. Proportion of Participants with at least a 4-fold rise in SBA-BR Antibody Titers Table D-7 shows the proportion of participants with a >_ 4-fold rise from baseline in Day 28 SBA antibody titers. Table D-7: Number and Percentage of Participants with a > 4-Fold Rise in Day 28 SBA Antibody Titers From Baseline Test Type %* TetraMenl(n"VN1) )(95% CI) %* Menomun(n"/N*) (95% CI) SBA (A) 80.4 (1028/1278) (78.16%, 82.58%) 84.5 (929/1099)" (82.26%, 86.62%) SBA (C) 88.5 (1131/1278) (86.62%, 90.20%) 89.6 (985/1099) (87.67%, 91.37%) SBA 73.6 (941/1278) (71.12%, 76.03%) 79.3 (872/1099) (76.83%, 81.70%) SBA (W-135 ) 89.4 (1142/1278) (87.54%, 91.00%) 94.3 (1036/1099) (92.72%, 95.57%) * %: n/N. t n: number of participants with > 4-fold rise from baseline titer. $ N: number of participants with blood draws within each serogroup. Proportion of Participants with Undetectable Titers ( 4-Fold Rise in Day 28 SBA-BR Antibody Titers Table D-8 shows the proportion of participants with undetectable titers (_ 4-Fold Rise in Day 28 SBA-BR Antibody Titers! in both treatment groups and for all vaccine serogroups, most participants with an undetectable ( 4-fold rise in Day 28 SBA titers. The proportions of participants with 107 an SBA titer 4-fold rise from baseline to Day 28 ranged from 90.7% to 100.0% in the TetraMenD group and from 96.9% to 99.3% in the Menomune group. Table D-8: Proportion of Participants with Undetectable Titers ( 24-Fold Rise in Day 28 SBA-BR Antibody Titers Test Type %* TetraM(n7Ns) :nD(95% CI) %* Menomune*(n7N$) (95%, CI) SBA (A) 100.0 (156/156) (98.10%, 100.00%) 99.3 (143/144) (96.19%, 99.98%) SBA (C) 99.4 (341/343) (97.91%, 99.93%) 97.7 (297/304) (95.311%, 99.07%) SBA 90.7 (253/279) (86.64%, 93.82%) 96.9 (221/228) ;. (93.78%, 98.76%) SBA (W-135) 96.5 (359/372) (94.10%, 98.13%) 99.1 (325/328) (97.35%, 99.81%) %: t n: number of participants with titers serogroup $N: number of participants with titers Table D-9 shows the SBA GMTs at baseline and on Day 28 after vaccination and the fold rises in SBA GMTs. 108 Table D-9: Summary of Geometric Mean of Antibody Titers (GMT) and Fold Rise of GMT by Serogroup (Per-protocol Population) Test Type Parameter* Bleed TetraMenD Menomu Nt GMT (95% CI)* Nt GMT (95% CI)* SerogroUD ASBA Titer DayO 1279 223.6 (199.86), 250.08 1099 203.9 230.23,23023) Dav28 1278 3896.6 (3646.33. 4164.11) 1099 4108. 9 (3827.43. 4411.15) Fold Rise Day 1278 16.0 (14.39-17.84) 1099 18.4 \ (16.39-20.67) SerogroUpC SBA Titer DayO 1279 57.2 (50.50, 64.73) 1099 51.8 (45.47, 59.11) Day 28 1278 3235.2 (3958.46)3537.76) 1099 4 3816.34) Fold Rise Day 28 1278 47.1 (41.74, 53.05) 1099 55.1 (48.53, 62.67) SerogrounY SBA Titer DayO 1279 122.9 (108.89. 138.72) 1099 127.4 (111.97, 145.03) Dav28 1278 1751.8 (1598.14. 1920.30) 1099 "2446. 7 (2235.36. 2677.93) Fold Rise Day 28 1278 12.3 (10-97. 13.68) 1099 16.6 (14.68-18.83) Seroerou p W-135SBA Titer DayO 1279 33.2 (2995 3 6 :7 3 ;36.73) 1099 31.( (27.90, 34.46) Day 28 1278 1270.7 (1171.59, 1378.22) 1099 1865..,.,, 5 (1717.28, 2026.48) Fold Rise Day 28 1278 31.4 (28.35. 34.70) 1099 48.9 (44.07. 54.30) * Titer or fold-rise, where fold rise= titer at Day 28/ Titer at Day 0 t N: number of participants with blood draws within each serogroup. Note: One Participant did not have a second blood sample done # 95% CI for the GMT is calculated based on an approximation to the normal distribution. Twenty-eight to 56 days after receiving the study vaccination, TetraMenD, the majority of participants experience a 4-fold rise in the SBA-BR antibody titer for each of the serogroups contained in the vaccine. The percentages of TetraMenD recipients obtaining a 4-fold rise in antibody titer are 80.4%, 88.5%, 73.6 %, and 89.4% for serogroups A, C, Y, and W-135, respectively. Higher pre-vaccination antibody levels are observed for 109 serogroup Y than for C or W-135. This may be related to the fact that serogroup.Y is currently the most common serogroup associated with invasive meningococcal disease in this age group in the U.S. and mat natural exposure to this serogroup may be more-common. Higher circulating antibody levels reflect recent natural exposure and may reduce the proportion of vaccine recipients exhibiting 4-fold or higher antibody responses. This appears to be the case for serogroup Y responses when compared to other serogroups. The 4-fold rise for serogroup Y is 73.6% compared with 88.5% for serogroup C and 89.4% for serogroup W-135. High pre-vaccination antibody levels are also observed for serogroup A. This may be the result of intermittent exposure over a prolonged period of time to several naturally occurring cross-reacting antigens. To further evaluate the impact of pre-existing titers and to investigate the rate of seroconversion (as defined by the proportion of vaccine recipients who achieve a 4-fold rise in antibody titer when the pre-vaccination titer for any serogroup is of the 4 serogroups contained in the vaccine. A titer of As previously discussed in another Study herein, based on observations in military recruits, Goldschneider proposed that a minimum titer of 1:4 using an SBA assay with a human complement source correlated with protection from invasive disease against Serogroup C. Baby rabbit complement is suggested as an alternative source, but meningococci appear to be more sensitive to the baby rabbit complement than human complement, resulting in higher measured antibody titers. Several authors have suggested that titers > 1:128 using the baby rabbit complement assay are predictive of protection while titers of 110 several months later showed mat these individuals are also protected, having achieved an antibody level >1:128. When this criterion is applied to all the serogroups contained in the vaccine, the percentages of participants receiving TetraMenD who achieve a post-vaccination SBA-BR titer > 1:128 arc 99.8%, 98.7%, 96.9%, and 97.1% for serogroups A, C, Y, and W- 135, respectively. Example 13 Study E Td Booster Study in Children Aged 10 to 18 This study compares the tetanus and diphtheria toxoid (Td) booster response in the group receiving the experimental tetravalent Meningococcal Diphtheria Conjugate vaccine, TetraMenD, concomitantly with Td to the response in the group receiving Td with placebo, as measured by the proportion of participants who have an acceptable response in their respective tetanus and diphtheria titers. An acceptable response is defined as, 28 days following vaccination, at least a 4-fold rise from baseline in participants with a predefined low pre-vaccination titer and at least a 2-fold rise from baseline in participants with a predefined high pre-vaccination titer. To compare the antibody response for serogroups A, C, Y, and W-135 in TetraMenD when administrated concomitantly with Td to the response when TetraMenD is administrated 28 days following Td vaccine, as measured by the proportion of participants with at least a 4-fold rise in titer to each serogroup. This is a randomized, modified double-blind, active-control multi-center, trial, with a total of 1024 participants randomized to one of two treatment groups: A and B; DayOVI Day 28V2 Day 56V3 Group A BS-l Td + TetraMenD BS-2 Placebo BS-3 Group B BS-1 Td + Placebo BS-2 TetraMenD BS-3 The age range of 11 to 17 years is chosen to capture those individuals who would normally receive Td vaccine as part of the routine childhood immunization schedule. In addition, this age range has been identified as high risk for development of invasive meningococcal 30 disease and would most likely be candidates for vaccination with the meningococcal 111 conjugate vaccine once licensed. In order to properly evaluate safety, a modified double-blind design using a placebo control is utilized. For the first visit, the vaccination nurse is =blinded and administered the vaccines in each arm according to protocol; TetraMenD (IM) or placebo in the right arm and Td in the left. For the second visit, each treatment group received the vaccine in the left arm. The evaluation nurse is blinded monitored local and systemic reactions and adverse events. The age range of 11 to 17 years is chosen to capture those individuals who would normally receive Td vaccine as part of the routine childhood immunization schedule., In addition, this age range has been identified as high risk for development of invasive meningococcal disease and would most likely be candidates for vaccination with the meningococcal conjugate vaccine once licensed. Blood specimens (at least 5 mL whole blood) for serologic testing are drawn on Day 0 prior to vaccination (baseline) and at Day 28 post-vaccination 1. There is a third blood draw for participants 28 days after visit 2. At each of these time points, sera are assayed for meningococcal serogroups A, C, Y, and W-135, anti-diphtheria antibody and anti-tetanus antibody. To evaluate antibody function in recipients of TetraMenD, all available specimens are assayed for SBA using baby rabbit complement (SBA-BR) against each vaccine serogroup. One immunologic endpoint is the proportion of participants in each treatment group with a >_4-fold rise in SBA-BR titer. Anti-diphtheria antibody levels are measured by the ability of the test sera to protect Vero cells from a diphtheria toxin challenge. Anti-tetanus antibody levels are measured by an indirect Enzyme Linked Immunosorbent Assay (ELISA). This study compares the antibody responses to TetraMenD for serogroups A, C, Y, and W-135 as measured by the GMTs in participants from an earlier study, Study C, who receive one dose of TetraMenD to the responses in participants who receive TetraMenD administered concomitantly with Td and 28 days following Td vaccination. Serum specimens for serologic analysis are obtained at baseline (Day 0) prior to vaccination and at Day 28 (window: +28 days) and 6 months after vaccination. Antibody titers to 112 tetanus toxoid and diphtheria toxoid (Td) vaccine are measured pre- and 28 days post vaccination. SBA-BR antibody titers for N. meningitidis serogroups A, C, Y, and W-135 are measured for ail available serum specimens pre- and 28 days post vaccination. Overall, the safety profile of Group A and Group B are comparable. The results of this Study are summarized in the following Tables. Table E-l summarizes GMT levels by Subject Age and Serogroup. * 1) Table E-l Summary of GMT by Subject Age and Serogroup Age Dose TetraMenD No. of Subjects Blood Day A GMT CGMT WGMT YGMT 10 1μg 1 0 2048.00 512.00 512.00 256.00 4μg 1 28 8192.00 1024.00 4096.00 1024.00 10μg 1 56 32768.00 4096.00 16384.00 8192.00 11 1 ug 273 0 186.38 63.35 23.06 140.97 4 μg 267 28 2331.86 513.33 339.73 775.64 10 μg 265 56 10668.96 2005.59 2285.81 2203.62 12 1μg 236 0 185.87 56.24 2723 138.56 4 μg 229 28 1672.07 516.67 280.33 752.00 10 μg 226 56 10030.01 2522.93 216424 2231.65 13 lμg 172 0 219.65 60.25 20.46 128.00 4μg 170 28 2562.84 664.66 372.52 898.74 10 μg 168 56 10493.02 2700.12 2346.72 2289.34 14 lμg 128 0 326.64 65.05 30.81 107.63 4μg 126 28 1896.19 597.26 388.88 752.50 10μg 126 56 9044.70 2375.94 2248.77 1885.79 15 1 g 101 0 223.17 83.07 47.00 114.69 4μg 95 28 2352.53 716.20 504.58. 776.05 10μg 94 56 9424.03 4575.06 2356.01 1988.48 16 lμg 71 0 393.36 46.83 24.11 70.56 4μg 70 28 2399.59 783.77 450.16 512.00 10 μg 69 56 8527.88 3154.48 1908.93 1833.75 17 1μg 35 0 358.47 107.10 28.41 79.58 4μg 35 28 2173.36 403.70 156.70 411.78 10μg 34 56 7398.11 3340.58 1418.93 1390.30 Table E-2 shows the numbers and proportions of participants with at least a 4-fold or 2-fold rise in tetanus and diphtheria antibody on Day 28. 113 Table E-2 Numbers and Proportions of Participants with at least a 4-fold or 2-fold rise in Tetanus and Diphtheria Antibody on Dav 28 Antigen Response Td+TetraMenD, Placebo(%=Pa) Td+Placebo, TetraMenD(%=Pb) Difference (Pb-Pa) 950 CIfor the%Difference Tetanus 2-Fold (Pre-titer >53 IU/mL) 0/24 (0.00) 2/23 (8.70) 4-Fold (Pre-titer <_53 iu> Total Responders 399/463 (86.18) 419/471 (88.96) 2.78 (-1.45,7.01) Diphtheria 2-Fold(Pre-titer >1.28 IU/mL) 44/47 (93.62) 42/49 (85.71) 4-Fold(Pre-titer 5 1.28 IU/mL) 419/419 (100.00) 416/425 (97.88) Total Responders 463/466 (99.36) 458/474 (96.62) -2.73 (-4.51,-0.95) Tetanus and Diphtheria Antibody Titers and SBA Antibody Titers for Serogroups A, C, Y,andW-135 Table E-2 shows the numbers and proportions of participants with at least a 4-fold or 2-fold 5 rise in tetanus and diphtheria antibody on Day 28. The differences In the proportions are: 2.78 and -2.73 for tetanus and diptheria, respectively. Table E-2: Total Number and Proportion of Participants with at least 4-Fold or 2-Fold Rise Response in Tetanus and Diphtheria Antibody on Day 28 Following the Tetanus and Diphtheria Vaccination, Primary Hypothesis l(Per-Protocol Population) Antigen Response Td+TetraMenD,Placebon/N (%=Pa) Td+PUcebo,Tetr*MenD n/N (%=Pb) Difference (Pb-Pa) 95% CI for the % Difference Tetanus 2-Fold (Pre-titer >5.3 IU/mL) 0/24 (0.00) 2/23 (8.70) 4-Fold (Pre-titer 5.3 IU/mL) 399/439(90.89) 417/448 (93.08) Total Responders 399/463 (86.18) 419/471 (88.96) 2.78 (-1.45,7.01) 114 Table £-2: Total Number and Proportion of Participants with at least 4-Fold or 2-Fold Rise Response in Tetanus and Diphtheria Antibody on Day 28 Following the Tetanus and Diphtheria Vaccination, Primary Hypothesis l(Per-Protocol Population) Antigen Response Td+TetraMenD,Placebon/N(%"Pi) Td+Placebo,TetraMenDn/N (%=Pb) Difference (Pb-Pt) 95% CI for the % Difference Diphtheria Z-Fold(Pre-titer >1.28 lU/mL) 44/47 (93.62) 42/49 (85.71) 4-Fold(Pre-titer Total Responders 463/466 (99.36) 458/474 (96.62) ; -2.73 (-4.51; 0.95) Table E-3 shows the numbers and proportions of participants with at least a 4-fold rise in antibody titer to serogroups A, C, Y, and W-135 on Day 28. Table E-3: Number and Proportion of Participants with a 4-Fold Rise in SBA-BR Titer on Day 28 Following the TetraMenD Vaccination, Primary Hypothesis 2 (Per-Protocol Population) Serogroup Td+TetraMenD,Placebon/N (%"Pa) Td+Placebo,TetraMenDn/N (%"Pb) Difference (Pb-Pa) 95% CI for the % Difference Serogroup A 419/466(89.91) 433/478(90.59) 0.67 (-3.11,4.46) Serogroup C 424/466(90.99) 394/478(82.43) -8.56 (-12.85; 4.27) Serogroup Y 399/466(85.62) 311/478(65.06) -20.56 (-25.89; 15.23) Serogroup W-135 448/466(96.14) 419/478(87.66) -8.48. (-11.91; 5.05) Table E-4 shows the number of participants with high diphtheria and tetanus titers at baseline and the number and proportion of participants with a 2-fold rise on Day 28. Table E-4: Number (%) of Participants with High Diphtheria and Tetanus Pre-Titers at Baseline and Number and Proportion of Participants with 2-Fold Rise on Day 28 Per-Protocol Population Td+TetraMenD,Placebo Td+PlaceboJetraMenD Baseline Titer 2-Fold Rise Baseline Titer 2-Fold Rise n/N % n/N % n/N % n/N % Tetanus> 5.3 M W 24/468 5.13 0/24 0.00 23/472 4.87 ! 2/23 8.70 Diphtheria > 1.28 M W 47/469 10.02 44/47 93.62 49/476 10.29 42/49 85.71 115 Table E-S shows the number of participants with low diphtheria and tetanus titers at baseline and the number and proportion of participants with a 4-fold rise on Day 28. Table E-5: Number (%) of Participants with Low Diphtheria and Tetanus Pre-Titers at Baseline and Number and Proportion of Participants with 4-Fold Rise on Day 28- Per Protocol Population Td+TetraMenD,Placebo Td+Placebo,TetraMenD Baseline Titer > 4-Fold Rise Baseline Titer 4-Fold Rise n/N % n/N % n/N % n/N % Tetanus 5 3 IU/ml 444/468 94.87 399/439 90.89 449/472 95.13 417/448 93.08 Diphtheria 116 Table E-6 shows the number and proportion of participants with a titer >1.0 IU/ml in tetanus and diphtheria antibody on Day 28 following tetanus and diphtheria vaccination given concomitantly with TetraMenD or Placebo. Table E-6: Number and Proportion of Participants with Titer 10 Tetanus IU/ml in An and Diphtheria tibody on Day 28 Following Tetanus and Diphtheria tion, ^Per-Protocol Population td+TetraMenP,Placebon/N (%=Pa) Td+Placebo,TetraMenDn/N(%=Pb) Difference (Pb-Pa) 95% CI for the % Difference Tetanus > LO r/ml 461/465 (99.14) 470/477 (98.53) -0.61 (-1.97,0.76) Diphtheria LO r/ml 467/467 (100.00) 474/476 (99.58) -0.42 (-1.00,0.16) Table E-7 shows the geometric mean an antibody titers (GMTs ) for tetanusan us and diphtheria on Day 28 following tetanus and diphtheria vaccination (given concomitantly with TetraMenD or Placebo). Table E-7: Comparison of Geometric Mean Antibody Titers(GMTs) for Tetanus and Diphtheria on Day 28 Following Tetanus and Diphtheria Vaccination, (Per-Protocol Population)[l] Td+TetraMenD .Placebo Td+Placebo, TetraMenD GMTa ( 95% CI) GMTb (95% CI) GMT Ratio GMTb/GMTa 95% CI for GMT Ratio Tetanus 11.46 (10.79,12.18) 13.56 (12.73,14.44) 1.18 (1.08,1.29) Diphtheria 304.69 (221.69,418.78) 10.60 (9.23,12.18) 0.03 (0.02,0.05) 117 Table E-8 shows the geometric mean antibody titers(GMTs) for SBA-BR for serogroups A, C, Y, and W-135 on Day 28 post TetraMenD vaccination. The GMT ratios are 0.92,0.42,0.39, and 0.32 for serogroups A, C, Y, and W-135, respectively. Table E-8: Comparison of Geometric Mean Antibody Titers for SBA -BR on Following the TetraMenD Vaccination, (Per-Protocol Population)[ll Day 28 Td+TetraMenD,Placebo Td+Placebo,TetraMenD GMTa (95% CI) GMTb ((95% CI) GMT Ratio GMTb/GMTa 95% CI for GMT Ratio Serogroup A . 11321.8 (10173.2,12600.0) 10391.4 1338.8] 0.92 (0.8,1.1) Serogroup C 5042.0 (4389.4,5791.7) 2136.0 (1810.8,2519.4) 0.42 (0.3,0.5) serogroup Y 3387.3 (2978.2,3852.5) 1331.3 (1170.2,1514.6) 0.39 (0.3,0.5) serogroup W-135 4175.8 (3702.1,4710.1) 1339.1 (1161.8,1543.4; 0.32 (0.3,0.4) 0.34, and 0.39 for serogroups A, C, Y, and W-135, respectively. Table E-9: Comparison of Geometric Mean Antibody Titers(GMTs) for SBA-BR on Day 28 Following the TetraMenD Vaccination in Group Td+TetraMenD Placebo to the Corresponding Results from Study C, (Per-Protocol Population) Td+TetraMenD,Placebo Study C GMTa ( 95% CI) GMT Study C ( 95% CI) GMT Ratio GMTmta02/ GMTa 95% CI for GMT Ratio Serogroup A 11321.8 (10173.2,12600.0) 5483.2 (4920.1,6110.7) 0.48 (0.4,0.6) Serogroup C 5042.0 (4389.4,5791.7) 1924.4 (1662.1,2228.0) 0.38 (0.3,0.5) Serogroup Y 3387.3 (2978.2,3852.5) 1322.3 (1161.9,1504.8) 0.39 (0.3,0.5) Serogroup W-135 4175.8 (3702.1,4710.1) 1407.2 (1232.1,1607.3) 0.34 (0.3,0.4) Table E-10 shows the geometric mean antibody titers (GMTs) for SBA-BR for serogroups A, C, Y, and W-135 on Day 28 post TetraMenD vaccination in the Td + Placebo, TetraMenD group and the corresponding results from study MTA02. The GMT ratios are 0.53,0.90,0.99, and 1.05 for serogroups A, C, Y, and W-135, respectively. 118 Table E-10: Comparison of ic Mean Antibody Titers (GMTs) for SBA-BR on Day 28 Following the TetraMenD Vaccination in Group B to the Corresponding Results from Study C, Observational Hypothesis (Per-Protocol Population)} 1] Td+Pbcebo,TetraMenD Study C GMTb ( 95% CI) GMT Study C (95% CI) GMT Ratio GMTmta 02/ GMTb 95% CI for GMT Ratio Serogtoup A 10391.4 (9523.1,11338.8) 5483.2 (4920.1,6110.7) 0.53 (0.5,0.6) Setogtoup C 2136.0 (1810.8,2519.4) 1924.4 (1662.1,2228.0) 0.90 (0.7,1.1) Serogtoup Y 1331.3 (1170.2,1514.6) 1322.3 (1161.9,1504.8) 0.99 (0.8,1.2) Serogtoup W-135 1339.1 (1161.8,1543.4) 1407.2 (1232.1,1607.3) 1.05 (0.9,1.3) to 1024). Table E-12 shows the distribution of SBA-BR antibody titers on Day 0 and Day 28 after the TetraMenD Vaccination by serogroup for the Per-Protocol Population (SBA-BR Titers 2048 to 524288) Table E-l 1: Distribution of SBA-BR Antibody Titers on Day 0 and Day 28 After die TetraMenD Vaccination by Setogtoup (Pet-Protocol Population) (SBA-BR Titers SBA Titers Test Type Test Date Group N n% n% n% n% n% n% n% n% n% SerogtoupA DayO Group A 470 90 19.1 13 2.8 5 1.1 2 0.4 9 1.9 255.3 60 12.8 68 14.5 97 20.6 Group B 478 5311.1 61.3 20.4 0 0.0 5 1.0 367.5 74 15.5 73 15.3 103 21.5 Day28 Group A 470 0 0.0 0 0.0 0 0.0 0 0.0 0 0.0 3 0.6 3 0.6 7 1.5 10 2.1 Group B 478 0 0.0 0 0.0 0 0.0 00.0 0 0.0 0 0.0 1 0.2 40.8 6 1.3 SerogtoupC DayO Group A 470 15132. 27 5.7 15 3.2 27 5.7 18 3.8 31 6.6 38 8.1 52 11.1 64 13.6 Group B 478 153 32. 31 6.5 20 4.2 13 2.7 12 2.5 55 11.5 49 10.3 42 8.8 45 9.4 119 Table E-ll: Distribution of SBA-BR Antibody Titers on Day 0 and Day 28 After the TetraMenD Vaccination by Serogroup (Per-Protocol Population)(SBA-BR Titer SBA Titers Test Type Test Date Group N n% n% n% n% n% n% n% n% n% Day 28 Group A 470 1 0.2 0 0.0 0 0.0 2 0.4 1 0.2 5 1.1 1123 265.5 39 8.3 Group B 478 2 0.4 2 0.4 2 0.4 9 1.9 4 0.8 20 42 35 73 52 10.9 67 14.0 Sero-groupY DayO Group A 470 10121.5 5 1.1 61.3 22 4.7 30 6.4 53 ...U-3 81 172 67 143 52 11.1 Group B 478 93 19.5 1 0.2 2 0.4 81.7 204.2 84 17.6 6914.4 71 14.9 6914.4 Day 28 Group A 470 1 0.2 1 0.2 1 0.2 2 0.4 3 0.6 7 1.5 12 2.6 23 4.9 65 13.8 Group B 478 4 0.8 3 0.6 1 0.2 2 0.4 5 1.0 204.2 387.9 6914.4 8517.8 Sero-groupW-135 DayO GroupA 470 205 43.6 30 6.4 17 3.6 33 7.0 37 7.9 41 39 83 31 6.6 17 3.6 Group B 478 213 44.6 29 6.1 9 1.9 14 2.9 265.4 6914.4 48 10.0 32 6.7 24 5.0 Day 28 GroupA 470 1 0.2 0 0.0 0 0.0 0 0.0 1 0.2 4 0.9 7 1.5 24 5.1 62 132 Group B 478 7 1.5 3 0.6 1 0.2 2 0.4 1 0.2 21 4.4 42 8.8 72 15.1 87 182 Group A: Vaccination 1 = Td + TetraMenD Vaccination 2 = Placebo Group B: Vaccination 1 = Td + Placebo Vaccination 2 = TetraMenD .. ; i >| 120 Table E-12: Vaccination Distribution of SBA-BR Antibody Titers on Day 0 and Day 28 After the TetraMenD i by Serogroup(Per-Protocol Population) (SRA-BR Titers 2048 to 524288) SBA Titers Miss- 2048 4096 8192 16384 32768 65536 131072 524288 ing. n n n n n n n n n Test Test Type Date Group N % % % % Sero- Day A 470 70 16 10 3 1 , 0 0 0 l group 0 14-9 3.4 2.1 0.6 (X2 0.0 0.0 0.0 0,2 A B 478 75 29 13 4 5 0 0 0 0 121 15.7 6.1 2.7 0.8 1.0 0.0 0.0 0.0 00 Day A 470 29 60 109 102 117 .,...17 10 0 3 28 6.2 12.8 23.2 21.7 24.9 3.6 2.1 0.0 OS B 478 38 75 112 147 83 7 5 0 0 7.9 15.7 23.4 30.8 17.4 1.5 1.0 0.0 0.0 Sero-Day A 470 36 4231 0 0 01 group 0 TJ_ 0.9 04 0J5 02 0.0 0.0 0.0 02 B 478 32 14 82 2 0 0 00 6.7 2.9 1.7 0.4 0.4 0.0 0.0 0.0 0.0 Day A 470 80 79 77 74 51 10 10 1 3 28 17.0 16.8 16.4 15.7 10.9 ,,, 2.1 2.1 0.2 0£ 122 B 478 79 62 59 36 35 5 9 0 0 16.5 13.0 12.3 7.5 7.3 1.0 1.9 00 0,0 Sero- Day A 470 37 9 4 2 0 0 0 0 1 group 0 7.9 1.9 0.9 0.4 0.0 0.0 0.0 0.0 02 B 478 35 15 6 5 0 0 0 0 0 7.3 3.1 1.3 1.0 0.0 0.0 0.0 0.0 0.0 Day A 470 74 114 77 56 28 12 0 3 28 15.7 24.3 16.4 11.9 6.0 0.2 0.4 0.0 0j6 B 478 113 73 47 15 3 0 0 0 0 2M 15.3 9,8 3A 0£ 0.0 0.0 0.0 0.0 Sero-Day A 470 15 3 1 0 0 . 123 group 0 3,2 0.6 0^2 W-135 B 478 11 1 2 0 0 0 0 0 0 2.3 0.2 0.4 0.0 0.0 0.0 0.0 QJO OJQ Day A 470 85 90 77 74 37 3 2 0 3 28 18.1 19.1 16.4 15.7 7.9 0.6; 0.4 0.0 0.6 124 Table £-12: Distribution of SBA-BR Antibody Titers on Day 0 and Day 28 After the TetraMenD Vaccination by Serogroup (Per-Protocol Population) (SBA-BR Titers 2048 to 524288) SBA Titers 2048 4096 8192 16384 32768 65536 131072 524288 Missing Test Tvde Test Date Group N n% n% n% n% n% n% ! n% n% n% B 478 109 22.8 60 12.6 39 8.2 19 4.0 12 2.5 2 : 0.4 1 0.2 0. 0.0 0 0.0 Group A: Vaccination 1 = Td + TetraMenD Vaccination 2 = Placebo • Group B: Vaccination 1 = Td + Placebo Vaccination 2 = TetraMenD Table £-13: Summary of A Diphtheria Titers (Per-Prol ntibody Titers: Distribution of Tetanus and ocol Population^ 11 Td+TetraMenD, Placebo Td+Placebo, TetraMenD Antibody Titer Test Date n/N (%) n/N.. ;Ht (%) Tetanus 0.1 IU/ml DayO 5/468 (1.1) 3/472 (0.6) Day 28 0/465 (0.0) 0/477 ,, (0.0) 20.1- Day 28 4/465 (0.9) 7/477 (1.5) 21.0 IU/ml DayO 182/468 (38.9) 195/472 (41.3) Day 28 461/465 (99.1) 470/477 (98.5) Diphtheria Day 28 0/467 (0.0) 0/476 (0.0) 20.1- Day 28 0/467 (0.0) 2/476 (0.4) 21.0 IU/ml DayO 127/469 (27.1) 106/476 (22.3) Day 28 467/467 (100.0) 474/476 (99.6) safyandinrnnogaiatycicMCV4v 125 adolescents. Briefly, in a multicenter randomized trial healthy 10-17 year olds (mean age Related studies were conducted to access the 12.9 years) received TetraMenD (MCV-4) + Td either concomitantly (n = 509), or at separate visits one month apart (n = 512). Safety assessments for the two vaccines, given separately and concomitantly, were collected on days 8 and 28 post-vaccination. Immune responses were assessed prior to and 4 weeks post-vaccination by antibody titers to diphtheria and tetanus, and serum bactericidal activity (SBA) to the meningococcal serogroups. The safety profile for subjects given Td alone was similar to that in subjects given Td + TetraMenD. Concomitant administration of Td + TetraMenD did not interfere with the immune response to either tetanus or diphtheria toxoids. SBA responses to the four serogroups are summarized in Table E-14 shown below. Table E-14: SBA response to the four serogroups Serogroup SBA (GMT) Concomitant I Administration Separate Administration Pre(N = 468) Post (N = 466) Pre(N=477) Post(N = 478) A 232 11313 228 10391 C 66 5059 57 2136 Y 124 3391 115 : 1331 W-135 26 4195 27 : 1339 This study shows that the co-administration of Td and TetraMenD was safe and well tolerated in the test subjects. Concomitant administration of TetraMenD + Td does not adversely affect immune responses to tetanus and diphtheria toxoids. The immune responses to serogroups C, Y, and W135 polysaccharide were enhanced when MCV-4 was co-administered with Td. The enhanced immune response observed in Ms study was surprising and unexpected. 127 Example 14 Comparison of Serum Bactericidal Assay with Baby Rabbit Complement and with Human Complement for N. Meningococcal Serogroups C, W-135 and Y A subset of serum samples from Study A, Stage HI, is used in this, study to compare the results obtained with SBA-BR titers with SBA-HC titers for Serogroups C, W-135 and Y. Subjects enrolled into this trial are at least 2 years of age but not yet 11 years of age and each is randomly assigned to one of the two vaccine groups. Approximately 5 mL of whole blood is collected from each subject at baseline (prior to vaccination) and on Day 28 post-vaccination. Blood specimens from subjects are centrifuged within 4 hours of collection. The serum is taken off the clot, transferred into labeled cry tubes and stored in a temperature-monitored freezer at -20°C or colder. All samples that are used in the analysis in this report are from paired sera obtained from the first subjects enrolled in the clinical study and that are of sufficient serum volume to complete all planned testing. All samples are from 2 year old and 3 year old subjects with the exception of a single 4 year old. There are 2 subjects in the intent-to-treat category. One of these is from„the TetraMenD vaccine group (Day 28 post-vaccination sample is collected on Day 24) and one is from the Menomune® vaccine group (Day 28 post-vaccination is collected on Day 9). Baby rabbit complement (Pel-Freez®, Clinical Systems LLC, Brown Deer, WI, product code 31038) is pre-screened for suitability in each of the serogroup specific assays. The criteria for suitability included an agreement with SBA-BR test results for a defined set of serum samples (within a 2-fold dilution) using a previously qualified lot of rabbit complement. Criteria for meeting predetermined titers for a reference serum and control samples are also used. Aliquots of 2.5 ml of the rabbit complement are stored at -70°C or colder until ready for use. Aliquots are thawed once and used or discarded. Serum from subjects enrolled is screened for anti-meningococcal polysaccharide IgG and IgM levels by ELISA and tested in the SBA-BR for functional antibodies to identify potential sources of complement for use in the SBA-H. Criteria established for selection of a human source of complement are the following; (1) lack of detectable antibody when assayed in the SBA-BR assay, (2) lack of intrinsic bactericidal activity, when used as the complement source in the assay, (3) acceptable performance when used as a complement source with a panel of negative control, using sera with previous negative test results 128 determined at an independent outside lab by Dr. Ray Borrow, and (4) acceptable reproducibility performance with a panel of 24 samples. Exogenous complement sources used in each of the serogroup specific assays are from different subjects. No complement sources are found to work for more man one serogroup. Also, the three complement sources used in the SBA assays are from a single donor per serogroup. Serogroup C Serum from several subjects with acceptably low ELISA values (less than 0.5 ug/ml for both IgG and IgM) demonstrated bactericidal activity. Serogroup Y The complement source for the serogroup Y SBA-H is selected from the subjects enrolled in the collection protocol. Serum from the source of complement displayed low-level serogroup Y IgG and IgM antibodies by ELISA and is negative in the SBA-BR assay. Serum from the source showed no intrinsic bactericidal activity when used in the SBA. Serogroup W-135 The complement source for the serogroup W-135 SBA-H is selected from the subjects enrolled in the collection protocol. Serum from the source of complement displayed low-level serogroup W-135 IgG and IgM antibodies by ELISA and is negative in the SBA-BR assay. Serum from the source showed no intrinsic bactericidal activity when used in the SBA. Serum Bactericidal Assays Briefly, meningococcal serogroups C, Y, and W-135 strains are obtained from the Centers for Disease Control, Atlanta, GA (CDC). Target strains of bacteria are prepared for use in the assays from freshly thawed working seed lot vials of serogroups C, Y and W-135. Each vial is used to streak a Thayer Martin plate that is incubated overnight at 37°C ± 0.5°C in 5% C02. The following day, isolated colonies are harvested with a sterile swab and used to inoculate the entire surface of fresh Thayer Martin plates that had been warmed to ambient temperature. Plates are incubated for 4 h at 37°C ± 0.5°C in 5% C02 to obtain a light veil of confluent bacterial growth that is harvested with sterile swabs and suspended in Dulbecco"s PBS + 0.1% Dextrose Buffer to a prescribed optical density (absorbance at 600 129 nm). A working solution with a prescribed concentration of bacteria is prepared in Dulbeccos PBS + 0.1% Dextrose Buffer, maintained at ambient temperature and used within 30 minutes of preparation. Test samples are heat-treated at 56°C for 30 minutes to inactivate endogenous complement. To all wells of a 96-well microtiter plate, Dulbecco"s PBS + 0.1% Dextrose Buffer is added, then test serum samples are dispensed in 2*fold serial dilutions across the plate leaving the final two columns of wells for complement and serum control wells. Columns on every plate included a complement column ([column 11] - serum/+complement) and a serum control column ([column 12]+seruml-complement). Freshly thawed complement is mixed with the working concentration of bacteria and the mixture is dispensed into all but the serum control wells of the microtiter plates. Bacteria without added complement are dispensed into the serum control wells. The plates are covered and placed on a plate-shaker for 1 minute then removed to a 37PC ± 0.5°C C02 incubator. Incubation times are 90 minutes for the serogroup A assay plates and 60 minutes for the serogroups C, Y, and W-135 assay plates. After incubation, 100 gl of agarose overlay medium at 50°C ± 1°C is carefully added to all wells avoiding air bubble formation. After a 10 minute period at ambient temperature with the microtiter plate lids ajar to avoid moisture formation, the plates are covered and removed to a dry (no "added humidity) 5% C02 incubator at 37°C ± 0.5°C for 20 ± 4 h. After this incubation, the number of bacterial colonies per well is counted. The average number of colonies per well for the complement controls wells is calculated and divided in half to obtain the 50% survival at To. The bactericidal titer of each unknown serum is expressed as the final reciprocal serum dilution yielding > 50% killing compared with the 50% survival value at T6. The starting dilution for samples in the SBA-BR is a 1:8 dilution. For the SBA-H, the starting dilution is lowered to a 1:4 dilution as described in the original assays. A comparison of the SBA-BR procedure for the serogroup A assay described herein with the Standardized SBA procedure (CDC) and with the SBA procedure as performed at the Manchester Public Health Laboratory Services, Meningococcal Reference Unit, Manchester, UK (PHLS) is provided as Table 14-1. 130 Table 14-1: Serum Bactericidal Assay Methods Comparison AvP-US CDC PHLS Frozen stock Greaves Somw.10% Glycerol Greaves Soln w 10% Glycerol Frozen in Glycerol (15%) broth Bactericidal buffer Dulbecco"s with 0.1% Glucose Dulbecco"s with 0.1% Glucose■ i Geys with 0.5% BSA Over night growth Media Thayer Martin (MR0232) Brain Heart Infusion w/1% Horse Serum Blood agar w/ 5% Horse Blood Over night Growth Conditions 37°Cw/5%C02 3T"Cw/5%C02 37°Cw/5%C02 Baby Rabbit (Pel-Freez) Baby Rabbit (Pel-Freez) Baby Rabbit (Pel-Freez) A Strain F8238 F8238 F8238 Assay day growth Media Thayer Martin (MR0232) Brain Heart Infusion w/1% Horse Serum Blood agar Assay day growth conditions 4hours37""Cw/5%C02 4hours37°Cw/5%C02 4hours37°Cw/5%C02 To targeted (per ml) 4000CFU/ml 4O00CFU/ml 80,000 CFTJ/ml Initial starting dilution of sen 1:4 1:4 1:2 Serum Treatment 56°C for 30 minutes 56°C for 30 minutes 56°C for 30 minutes Total volume at incubation step 50 .tl 50 .tl 40 .u Serum mixture as % total (vol.) 50%(25U) .50%(25gl) 50%(20gl) Cell suspension % (volume) 25%(12.5gl) 25%(12.5gl)..i lit 25%(10gl) Complement % (volume) 25%(12.5gl) 25%(12.5gl) 25%(10tl) CFU/well in rim mixture (the or.) 50 50 800 Final starting dilution 1:8 1:8 1:4 Serum Incubation conditions 37°Cw/5%C02for90 minutes 37°C for 90 minutes 37°Cw/oC02for90 minutes Oversight Iacabation netted 100 .tl TSB Agar overlay added (in 96 well plates) - 37°Cw/ 5%C02 100 tl TSB Noble Agar overlay added -37°Cw/5%C02 (in 96 well plates) 10 .tl on Agar Plates (Tik Method) 37-C To conditions 37°C for 90 minutes(i.e. Complement ControlAverage) 37°C for 90 minutes (i.e. Complement Control Average) Plated prior to 90 minuteincubationOvernight at 37°C w/ 5%C02 Endpoint Titer 50% Killing 50% Killing 50% Killing A reference serum is obtained from Dr. George Carlone, CDC (CDC; donor-R21654-3430107) as lyophilized powder in vials, which are stored at 2°C to 8°C until used. When needed, vials are each rehydrated with 0.5 ml sterile water and stored at -80°C to -40°C as 100 ul working aliquots. The titer of the reference serum when reconstituted under these conditions is 1:256 + 1 two-fold dilution in the standardized SBA-BR for serogroups A, C, Y, and W-135. Reference serum samples are run twice on different plates of the daily set of plates. Group-specific rabbit antisera for serogroups A, C, Y, and W-l 35 are purchased from Difco as lyophilized powder in vials, that are stored at 2° to 8°C until used. When needed, each vial is rehydrated with 1 ml sterile water and stored at -80°C to -40°C as 50 ul aliquots for use as quality control samples in the SBA. 131 The results of the Serum Bactericidal Assay using baby rabbit complement (SBA-BR) provided herein for the determination of complement-mediated anti-polysaccharide bactericidal activity to Neisseria meningitidis serogroups C, Y, and W-135 in clinical-Serum samples is fully validated for precision, dilutability (linearity), specificity and limit of detection. The SBA-H assay (for Serogroup C) is repeated on five consecutive days with an identical set of serum samples to establish the precision of the assay. Calculation of sensitivity and specificity of the SBA-BR Titers obtained in the SBA-BR are classified as true positive (TP) "(and false positive [FP]) and true negative (TN) (and false negative [FN]) using the SBA-H benchmark titers of 1:4 and 1:8. Sensitivity is calculated as TP/(TP + FN) and specificity is calculated as TN/(TN + FP). The results of these calculations are expressed as percentages. SBA Titer Distribution Comparison of SBA-BR versus SBA-H The pre- and twenty-eight day post-immunization SBA titers are shown in Tables 1 and 4 for serogroup C, Tables 2 and 5 for serogroup Y, and Tables 3 and 6 for serogroup W-135. Summarized in the following subsections is an analysis of the pre- and post-immunization SBA titers comparing the results obtained for the two sources of complement (BR versus H). Serogroup C SBA Titer Distribution Of the 101 pre-immunization serum samples, 63 are negative as defined by having a SBA-H titer of = 1:8). The false positive rate using a SBA-BR cut off titer of "1:4) are negative by SBA-BR ( In the post-immunization sera, 48 samples are negative by SBA-H, and only 11 are negative by SBA-BR. Of the 11 samples that are negative by SBA-BR, 3 arc positive by SBA-H. Seventeen of 51 post-immunization samples (32%) in the conjugate group are negative by SBA-H, but positive by SBA-BR (>= 1:8). For the polysaccharide group, 23 6f 50 post- 132 immunization samples (46%) are negative by SBA-H, but positive by SBA-BR titer (>_ 1:8). In terms of positive responses in the post immunization sera, 90 of 101 (89%) of samples are positive by SBA-BR (>= 1:8) but only 53 of 101 (52%) are positive by SBA-H (>= 1:4). There is a notable difference in the positive response rates when comparing the SB A titers (BR versus H) obtained for the two vaccine groups. For the 51 post-immunization samples in the conjugate group, 33 of 51 (65%) are positive by SBA-H (>= 1:4) and by SBA-BR (>= 1:8). Agreement between the SBA titers (BR versus H) improves at a SBA-BR threshold titer of >= 1:64 and higher. Of the 50 post-immunization samples in the polysaccharide group, 17 of 50 (34%) are positive by SBA-H (>= 1:4) and by SBA-BR (>= 1:8). Agreement between the SBA titers (BR versus H) improves at SBA-BR threshold titer >=1:512 and higher. Serogroup Y SBA Titer Distribution Unlike the serogroup C pre-immunization sera, only 9 of the serogroup Y pre-immunization samples are negative as defined by having an SBA-H titer = 1:8). The false positive rate using a SBA-BR cut off titer of = 1:4) but negative by SBA-BR ( There are no post-immunization serum samples that had a SBA-H titer = 1:8). As noted for serogroup C, there is a difference in the proportion of false negative results.. In the conjugate group, 5 of 48 samples (9%) are negative by SBA-H ( There is good agreement between the two SBA titers (BR versus.H) for positive responses in the post-immunization sera for serogroup Y. For the total set of 100 samples, all 100 post-immunization samples had SBA-BR titers >= 1:8, and 81 of 100 had SBA-H titers of >= 1:4. As noted for the SBA responses for serogroup C, there is better correlation between the SBA titers (BR versus H) in the conjugate group compared to the SBA titers (BR versus 133 H) obtained for the polysaccharide group. Of the 48 post -mimumzation samples in the conjugate group, 43 (90%) are positive by SBA-H (>= 1:4) and by SBA-BR (>=1:8). Only 1 of 48 samples had a SBA-BR titer less than 1:32, and that sample is positive by SBA-H (>= 1:4). The agreement between the SBA titers (BR versus H) is not as good in the polysaccharide group. Only 38 of 52 (73%) had post-immunization SBA-H titers >=1:4 and a SBA-BR titer >=1:8. Agreement between the SBA titers (BR versus H) in the post-immunization sera for the polysaccharide group improves at a SBA-BR titers of >=1:1!28. Serogroup W-135 SBA Titer Distribution For serogroup W-135, 54 of 100 (54%) are negative where both the SBA-H titer is =1:8). The false positive rate using a SBA-BR cut off titer of = 1:4) but are negative by SBA-BR ( Three post-immunization samples are negative by SBA-H (= 1:8). In the conjugate group, 11 of 47 samples (23%) are negative by SBA-H but positive by SBA-BR. In the polysaccharide group, 28 of 53 samples (53%) are negative by SBA-H but positive by SBA-BR. The agreement between the post-immunization SBA-BR and SBA= 1:4 and all are positive by SBA-BR (>= 1:8). All samples from the conjugate group had post vaccination SBA-BR titers >= 1:32. For the post-immunization titers for the polysaccharide group, the correlation between the two titers is not as good, only 22 of 53 (42%) had an SBA-H titer >= 1:4 and 50 of 53 (94%) had a SBA-BR titer >= 1:8. 134 Table 1. Comparison of the SBA-BR titer in sera positive and negative by SBA-H for serogroup C 1/SBA-BRtiter No. of sera with indicated SBA-H titer: Pre-immunization 28-day " TetraMenD Menomune* Combined =4 =4 =4 =4 8 4 0 1 0 1 0 2 0 16 1 1 1 0 1 1 2 1 32 2 0 5 3 1 1 6 4 64 4 0 4 6 5 2 9 8 128 3 2 3 9 8 :!"2 11 11 256 11 1 1 3 4 3 5 6 512 1 0 0 5 1 3 1 8 1024 0 0 2 6 1 4 3 10 2048 1 0 0 1 1 0 1 1 4096 0 0 0 0 0 1 0 1 Total 90 11 18 33 30 20 48 53 -{III Table 2. Comparison of the SBA-BR titer in sera positive and negative by SBA-H for serogroup T 1/SBA-BRtiter No. of sera with SBA-H titer: 28-dav Pri immuni tzation TetraMenD Menomune Combined =4 =4 =4 =4 8 1 1 0 1 0 0 0 1 16 4 2 0 0 0 0 0 0 32 10 6 1 3 2 4 3 64 14 6 3 4 2 5 5 128 15 12 9 4 6 5 15 256 7 9 13 2 16 3 29 512 1 0 7 1 6 2 13 1024 0 0 0 5 0 4 0 9 2048 0 1 0 3 0 :!"!1 0 4 4096 0 0 0 1 0 1 0 2 Total 61 39 5 43 14 38 19 81 Table 3. Comparison of the SBA-BR titer in sera positive and negative by SBA-H for serogroupw-135 1/SBA-BRtiter No. of sera with indicated SBA-H then 28-day post-immunization 135 Pn imntuni 6-ization TetraMenD Menaomunel|> Combined «4 =M =4 =4 8 1 3 0. 0 0 0 0 0 16 3 0 0 0 1 0 1 0 32 2 0 0 1 0 0 0 1 64 11 2 1 2 3 3 4 5 128 7 1 2 2 7 2 9 4 256 3 2 4 3 6 5 10 8 512 0 0 4 13 5 4 9 17 1024 0 0 0 3 5 ,■•3 5 6 2048 0 0 0 11 1 5 1 16 4096 0 0 0 1 0 0 0 1 Total 81 19 11 36 31 22 42 58 Table 4. Summary of distribution of serogroup C titers measured by the SBA-BR and the SBA-H 1/bactericidaltiter No. of samples" (% of pre- post-) with indicated titer by: SBA-BR SBA-H Pre- P 4 2(1.98) 1 (2.00) 1(1.96) 8 4 (3.96) 1(2.00) 1 (1.96) 0 2 (4.00) 1(1.96) 16 2(1.98) 2(4.00) 1 (1.96) 3 (2.97) 2 (4.00) 5 (9.80) 32 2(1.98) 2(4.00) 8(15.69) 1 (0.99) 3 (6.00) 3 (5.88) 64 4 (3.96) 7 (14.00) 10(19.61) 1 (0.99) 0 5 (9.80) 128 5 (4.95) 10(20.00) 12 (23.53) 3 (2.97) 3 (6.00) 5 (9.80) 256 12 (11.88) 7(14.00) 4 (7.84) 1 (0.99) 1 (2.00) 5 (9.80) 512 1 (0.99) 4(8.00) 5 (9.8) 0 .... 5(10.00) 2 (3.92) 1024 0 5 (10.00) 8(15.69) 0 1 (2.00) 5 (9.80) 2048 1 (0.99) 1(2.00) 1 (1.96) 0 0 1(1.96) 4096 0 1(2.00) 0 0 1 (2.00) 0 8192 0 0 0 0 1 (2.00) 0 Total number of samples is 101. Table 5. Summary of distribution of serogroup Y titers measured by the 8BA-BR and the SBA-H 1/bactericidaltiter No. of samples1 (% of pre- or ost-) with indicated titer by: CRA.RP «n*.n Post-imm. Post-imm. 136 Pre-imm. Menomune* TetraMenD Pre-imm. Menomune TetraMenD 4 1 (1.Q0) 0 1 (2.08) 8 2 (2.00) 0 1(2.08) 3 (3.00) 1 ;(1.92) 4 (8.33) 16 6 (6.00) 0 0 11 (11.00) ;, 12 (23.08) 2 (4.17) 32 16 (16.00) 5 (9.62) 2 (4.17) 12 (12.00) 11(21.15) 11 (22.92) 64 20 (20.00) 6 (11.54) 4(8.33) 5 (5.00) 9(17.31) 5 (10.42) 128 27 (27.00) 10 (19.23) 10 (20.83) 6 (6.00). 2(3.85) 8 (16.67) 256 16 (16.00) 18 (34.62) 14(29.17) 1(1.00) " " 1(1.92) 6 (12.50) 512 1 (1.00) 7 (13.46) 8 (16.67) 0 1(1.92) 4 (8.33) 1024 0 4(7.69) 5 (10.42) 0 1(1.92) 2 (4.17) 2048 1 (1.00) 1 (1.92) 3 (6.25) 0 0 0 4096 0 1 (1.92) 1 (2.08) 0 0 0 Total number of samples is 100. Table 6. Summary of distribution of serogroup W-13S titers measured by the SBA-BR and the SBA-H 1/bactericidaltiter Ho. of samples1 (% of pre- or post-) with indicated titer by: SBA-BR SBA-H Pre-imm. Post-imm. Prelum. " Post- imm. Menomune® TetraMenD Menomune® TetraMenD 4 4 (4.00) 5 (9.43) 6 (12.77) 8 4 (4.00) 0 0 10 (10 00) 7 (13.21) 2 (4.26) 16 3 (3.00) 1 (1.89) 0 2 (2.00), 5 (9.43) 11 (23.40) 32 2 (2.00) 0 1 (2.13) 3 (3.00) 1 (1.89) 5 (10.64) 64 13 (13 00) 6 (11.32) 3 (6.38) 0 3 (5.66) 2 (4.26) 137 128 8 (8.00) 9 (16.98) 4(8.51) 0 0 5 (10.64) 256 5 (5.00) 11(20.75) 7 (14.89) 0 0 3 (6.38) 512 0 9 (16.98) 17 (36.17) 0 1 (1.89) 1 (2.13) 1024 0 8 (15.09) 3 (6.38) 0 0 1 (2.13) 2048 0 6(11.32) 11 (23.40) 0 0 0 4096 0 0 1(2.13) 0 0 0 otal number of sam samples is 100. Sensitivity and Specificity Comparison of the SBA-BR and SBA-H Titers SBA-BR titers are compared to the SBA-H protective titers of 1:4 and! 1:8 in performing sensitivity and specificity assessments between the two sets of titers. Both pre- and post-immunization sera are used in this analysis. Using the SBA-H benchmark titers of 1:4 and 1:8, specificity and sensitivity are calculated for all three serogroups and are summarized in Tables 7,9 and 10. The analysis of sensitivity and specificity are discussed in turn for each serogroup. For serogroup C, the sensitivity is greater than 80% for SBA-BR threshold titers of 1:8,1:16, and 1:32 relative to both a 1:4 and 1:8 SBA-H titer. However, the specificity at these SBA-BR titers is less than 60%. Specificity increased above 60% at a SBA-BR titer of 1:64, and above 70% at a SBA-BR titer of 1:128. For these latter two SBA-BR titers, the specificity begins to drop off. At a SBA-BR threshold titer of 1:64, the sensitivity is between 75 and 78%, but at a SBA-BR titer 1:128, sensitivity falls to between 62 and 65%. Specificity continues to improve at SBA-BR titers > 1:64 ranging from 73% up to 83% for 1:128 and 1:256, respectively. However, sensitivity falls from 43% to less than 20%. The SBA-BR titer for serogroup C with the best balance between sensitivity and specificity fells in a range of SBA-BR titers between 1:32 and 1:128. The sensitivity and specificity results for serogroup C are found to be quite comparable to the results obtained by Santos GF, et al., 2001. Clin. Diaen. Lab. Immunol. 8:616-623, obtained by different set of serum samples and reagents (Table 8). With respect to Santos"s results, the best balance of sensitivity and specificity is observed between the SBA-BR titers of 1:64 and 1:128 versus both the SBA-H titers of 1:4 and 1:8. Table 7. Sensitivity and Specificity of the SBA-BR at Protective Titers in the SBA-H for Serogroup C SBA-H titer of >=1;4 SBA-H titer of >=1:8 138 1/SB A-BR titer SBA-H titer of >=1:4 SBA-H titer of >°1:8 y p Sensi o S.eci&l oo Sensi o sieci °o 84 56 88 56 32 81 58 85 58 64 75 v4 78 64 128 62 73 65. 73 256 42 83 43 83 512 31 95 33 95 1024 19 96 20 96 Table 8. Sensitivity and Specificity of the SBA-BR at Protective Titers in the SBA-H for Serogroup C as reported by Santos et al. 2001. CI. Diaen. Lab. Immunol. 8:616-623. 1/SBA-BR titer SBA-H titer of >= 1:4 SBA-H titer of >= 1:8 Sensitivity % Specificity % Sensitivity % Specificity % 32 85 61 91 58 64 78 73 86 68 128 69 83 78 81 256 54 87 63 88 512 41 92 49 94 For serogroup Y, sensitivity is highest for SBA-BR threshold titers ranging from 1:8 to 1:64, but, as expected, drops off at higher SBA-BR threshold titers. Specificity results for serogroup Y start out much lower compared to the results for serogroup C, and do hot reach a level of greater than 50% until a threshold SBA-BR titer of 1:128. The SBA-BR titer that is best balanced for sensitivity and specificity for serogroup Y falls in a range between 1:64 and 1:256. At 1:256, the sensitivity drops off to approximately 55%, but specificity increases from the mid-30% region to approximately 82-83%. Table 9. Sensitivity and Specificity of the SBA-BR at Protective Titers in the SBA-H for Serogroup Y SBA-H titer of >= 1:4 SBA-H titer of >= 1:8 Sensitivity (%) Specificity (%) Sensitivity (%) Specificity (%) 8 98 11 98 11 16 97 12 97 12 32 95 17 95 17 64 87 35 87 34 128 78 59 78 57 256 56 84 55 82 512 56 84 55 82 139 1024 13 100 14 .100 For serogroup W135, the values for sensitivity follow more closely to the values obtained for serogroup C, but the overall pattern is the same for all three serogroups. Sensitivity starts out high at a SBA-BR threshold titer of 1:8 and drops off at titers >=* 1:128. Likewise, specificity starts out low at a SBA-BR titer of 1:8 begins to level out at a titer of 1:256. As observed for serogroup Y, the SBA-BR with the best balance between sensitivity and specificity for serogroup W135 falls in a range between 1:64 and 1:256. Table 10. Sensitivity and Specificity of the SBA-BR at Protective Titers in the SBA-H for Serogroup W-135 SBA-H titer of >= 1:4 SBA-H titer of >= 1:8 Sensitivity (%) Specificity (%) Sensitivity (%) Specificity (%) 8 86 46 87 43 16 82 48 82 44 32 82 50 82 47 64 80 52 a 49 1/SBA-BR titer 71 64 73 61 256 65 77 64 72 512 52 88 50 83 1024 30 95 34 94 in Table 1 lare the proportionoffo four-fold fold rise inSBA titers usingboth baby rabbit complement or human complement for serogroups C, Y, and W135 relative to the post-immunization SBA-BR titer. This analysis is performed separately on the conjugate group, TetraMenD, and the polysaccharide group, Menomune®, and both sets of analysis are included in Table 11. There are some observable differences in the four-four rise patterns comparing the bactericidal responses induced to the three serogroups and for the two vaccine groups. The response patterns are discussed in turn for each serogroup and for both vaccine groups. Table 11. Stratified Comparative Ratios to a 4-Fold Rise in Meningococcal 20 Polysaccharide Titers Determined by SBA-BR and SBA-H1 Serogroup C Serogroup D Y Serogroup W-135 Tetra vlenD Menomune® Tetra MenD Menon Dune® Tetra MenD Menon uine® 1/SBA- SBA-BR SBA-H SBA-BR SBA-H SBA-BR SBA-H SBA-BR SBA-H SBA-BR SBA-H SBA-BR SBA-H 140 BR titer 8 0/1 (0%) 0/1 (0%) 0/1 (0%) 0/1 (0%) 0/1 (0%) 1/1 (100%) na na na na na na 16 0/1 (0%) 0/1 (0%) 0/2 (0%) 1/2 (50%) Na na na na na na 0/1 (0%) 0/1 (0%) 32 7/8 (87%) 3/8 (37%) 2/2 (100%) 1/2 (50%) 1/2 (50%) 0/2 (0%) 2/5 (40%) 1/5 (20%) 0/1 (0%) i 1/1 (100%) na na 64 9/10 (90%) 6/10 (60%) 6/7 (86%) 2/7 (29%) 1/4 (25%) 0/4 (0%) 2/6 (33%) 0/6 (0%) 3/3 (100%) 0/3 (0%) 6/6 (100%) 0/6 (0%) 128 11/12 (92%) 7/12 (58%) 8/10 (80%) 2/10 (20%) 5/10 (50%) 6/10 (60%) 4/10 (40%) 2/10 (20%) .""2/4 (50%) 1/4 (25%) 8/9 (89%) 2/9 (22%) >=256 11/18 (61%) 14/18 (78%) 12/18 (67%) 7/18 (39%) 28/31 (90%) 23/31 (74%) 17/31 (55%) 18/31 (58%) 36/39 (92%) 23/39 (59%) 32/34 (94%) 6/34 (18%) Total 38/51 30/51 a/sO 14/50 35/48 30/48 25/52 21/52 41/47 " 25/47 46/53 8/53 "The table shows as a ratio (and percentage) the 4-fold rise in SBA titer as determined in each assay (from paired samples pre-immunization and 28-day post-immunization) .. stratified by SBA-BR titer, vaccine and serogroup. For serogroup C, there is close agreement in the four-fold rise between SBA-BR versus SBA-H for the conjugate group. Within this vaccine group, there appears to be a trend that at low post-immunization titers, e.g. 1:32 -1:128, the SBA-H four-fold rise is lagging behind the four-fold rise in SBA-BR. But, at post-immunization SBA-BR titers >=* 1:256, the number of subjects achieving a four-fold rise by SBA-H appears to be greater than the number of subjects achieving a four-fold rise by SBA-BR. This difference in the fold rises comparing the two complement sources is small, and may be due to higher pre-immunization SBA-BR titers that alter the percentage of achieving a four-fold rise by SBA-BR. For the polysaccharide group, the agreement between the four-fold rise between SBA-BR versus SBA-H is not as close as it is for the conjugate group. Also, there is no notable trend that the four-fold rise by SBA-H becomes more sensitive at higher post-immunization SBA-BR titers than is observed for the conjugate group. For serogroup Y, the agreement between the four-fold rise by SBA-H and SBA-BR is very close for both vaccine groups. There are very few post-immunization SBA-BR titers less than 1:32 for either vaccine group compared to the post-immunization SBA-BR titers for serogroup C. For this reason, the proportion of subjects achieving a four-fold rise in both SBA-BR and SBA-H for serogroup Y occurs at a higher post-immunization SBA-BR titer compared to "serogroup C. For serogroup Y, the proportion of four-fold rise increases to >= 141 50% at a post-immunization SBA-BR titer of 1:128 for the conjugate group, whereas for serogroup C the threshold SBA-BR titer is 1:32 for the conjugate group. The agreement between four-fold rise by SBA-H and SBA-BR for serogroup W135 is not as close compared to the other two serogroups. As observed for serogroup Y, there are a limited number of subjects with post-immunization SBA-BR titers less than 1:32 for either vaccine group. The agreement between the four-fold rise in SBA titers (BR versus H) occurs at SBA-BR titers >= 1:256. As noted for serogroup C, there is a difference in the proportion of four-fold rises (BR versus H) between the two vaccine groups that is less evident for serogroup Y. The agreement between the four-fold rise in the serogroup W135 SBA titers (BR versus H) is poorest in the polysaccharide group compared to the four-fold rise in SBA titers (BR versus H) by the polysaccharide vaccine for the two other serogroups. The Serum Bactericidal Assay with baby rabbit complement (SBA-BR) is compared to the corresponding SBA using human complement (SBA-H) for measuring titers in serum samples from 2 to 3 year old subjects vaccinated with either the licensed quadrivalent meningococcal polysaccharide vaccine (Menomune®) or an experimental quadrivalent meningococcal polysaccharide conjugate vaccine (TetraMenD). Human complement sources for serogroups C, Y, and W135 are identified and used to support this comparison in the SBA. The SBA results from this comparative study are analyzed by two approaches. In one approach the SBA-BR and SBA-H data obtained by measuring the pre- and post-immunization titers for both vaccine groups are pooled for analysis. In the second approach, the pre- and post-immunization titers from the two vaccine groups are analyzed separately. One of the goals of this study is to describe the SBA-BR serum titer that best correlates to a negative SBA-H serum titer. A second goal is to determine the titer using baby rabbit complement that best correlated with a positive titer using human complement in the assay as a correlate of protection for serogroup C and to extrapolate to the protective bactericidal titers for serogroups Y and W135. Other laboratories have published results attempting to establish a protective threshold correlate for the SBA-BR for serogroup C. The results of this study will be compared to those published results. Lastly, the four-fold rise in SBA titers measured in pre- and post-immunization sera are compared for the two complement sources. 142 A correlation of a SBA titer to protection against disease has only been established for serogroup C. The SBA correlate of protection for serogroup C is determined using human complement in the SBA assay. For the other serogroups an assumption will be made that the SBA-H correlate of protection for serogroup C (SBA titer of 1:4) applies for the other serogroups. Defining a SBA-BR titers) that correlates to the SBA titer of 1:4 for serogroup C may differ between serogroups. In terms of defining a SBA-BR titer that best correlates to a negative SBA-H serum titer, a SBA-BR titer of Based upon the SBA titers (BR versus H) generated in this study, the false positive rate for serogroup C using a SBA-BR cut off titer of ...tit improves the false positive rate as follows: at >=1:16 the false positive rate decreases to 26%, at >= 1:32 the false positive rate decreases to 24%, at >= 1:64, the false positive rate decreases to 22%,at>= 1:128 the false positive rate decreases to 18%, at >=1:256 the false positive rate decreases to 14%, and at >= 1 ;5 L2 the false positive rate decreases to 2%. Increasing the SBA-BR cut off titer does serve to improve the accuracy of defining a negative titer that corresponds to a SBA-H titer of than 1:32, the sensitivity drops below £0%. However, specificity of the assay at cut off titers of 1:8,1:16, and 1:32 is at a minimum, ranging from 51 to 58%. A balance is made between sensitivity, specificity and false positive rates in selecting a cut off titer that correlates to a negative titer in the human complement assay. The assignment of 1:32 as the cut off titer for the SBA-BR would result in unnecessarily rejecting true positive responders. The results of this study indicate that a SBA-BR titer of >= 1:16 may be a more appropriate cut off titer. It is minimally 2-dilutions above the titer deemed protective based upon both the WHO/CDC study analysis ( 143 .-.lit Identification of the protective cut off titer in the assays for serogroups Wl 35 and Y are derived by assuming that bactericidal antibody protection is analogous with serogroup C disease and the bactericidal titers that correspond to a negative titer in the human complement assay. For serogroup Y, the false positive rate using a SBA-BR cut off titer of = 1:128, the false positive rates for the two serogroup assays become quite comparable. Such high cut off titers, hoarer, may overstate the threshold titers for a positive response. Based upon the sensitivity and specificity analysis, sensitivity is maximized at SBA-BR cut off titers of 1:8 to 1:32, where sensitivity ranged from 95 to 98%. However, as with serogroup C, specificity at these SBA-BR titers is correspondingly low, ranging from 11 to 18%. At the next highest SBA-BR titer, 1:64, sensitivity decreases from 95% to 88%, but the specificity sharply increases to 35%. A cut off titer of For serogroup W135, the false positive rate at a SBA-BR cut off titer of Having identified titers for the three serogroups that correspond to negative titers in the human complement assay, SBA-BR titers above these levels are analyzed for a threshold 144 titer for consideration of a positive response. For serogroup C me threshold titer for a positive response is >= 1:16, for serogroup Y the threshold titer for a positive response is >=, 1:64, and for serogroup W135 the threshold titer for a positive response is >= lc64. It appears that a threshold SBA-BR titers of >= 1:128 for serogroup C provides good assurance mat a protective titer is achieved, relative to either a SBA-H titer of 1:4 or 1:8 and correlates of efficacy SBA-H titer of 1:4 for serogroup C. This threshold titer compares well with the analysis made on the WHO/CDC data set for serogroup C, and to the data set of Santos. As noted in both of these studies, titers >= 1:128 are highly predictive of protection, but SBA-BR titers less than 1:128 may also be protective. For the WHO/CDC and the Santos data set, SBA-BR titers of 1:8,1:16,1:32,1:64 are referred to as the equivocal titers. Since SBA-BR titers less than 1:16 for the data set presented herein for serogroup C are regarded as negative, the equivocal titers for this analysis is 1:16 to 1:64, which is a subset of the other two studies. In all of these analyses, SBA-BR titers are being compared to SBA-H titers (1:4 or 1:8) that correlate to natural protection data that is ,,- More recently, efforts have been made to correlate the United Kingdom efficacy data for the monovalent C conjugates directly to a SBA-BR titer (Miller E, et al., 2002, Vaccine 20:S58-S67). In this analysis both SBA-BR titers of >= 1:8 and>= 1:128 are found to correlate well with the efficacy data that has been collected thus far for 15 to 17 year old subjects vaccinated with one dose of the monovalent C conjugates. However, when Miller and colleagues performed the same analysis for the toddler age group (12 to 30 months of age) they found very good agreement between SBA-BR titers of >= 1:8 with efficacy, but at SBA-BR titers of >= 1:128 the agreement is not as close. Miller presented additional data at the 13th International Pathogenic Neisseria Conference, September 1-6,2002 in Oslo, Norway where the predicted efficacy of subjects achieving a SBA-BR titers >= 1:64, one-month post vaccination, are outside the 95% confidence interval of the observed efficacy for this age group. These data help support the notion that SBA-BR titers in the equivocal region of 1:8 to 1:64 may lend assurance of protection. Based upon the analysis for this study, SBA-BR titers of 1:16 to 1:64 may likewise lend assurance of protection against serogroup C. 145 ..lit The serogroup Y assay at a SBA-BR titer of 1:64 has a specificity of only 35%, but as the cut off titer is increased to 1:128 and 1:256, specificity increases to 59% and 84%, respectively. A threshold titer of >= 1:256 provides good assurance of a protective titer in the human complement assay of 1:4 and 1:8. However, sensitivity and specificity are better balanced at a threshold titer of 1:128 for serogroup Y. The range of SBA-BR titers of 1:64 to 1:128 for serogroup Y represent the equivocal range of titers compared to the corresponding range of SBA-BR titers of 1:16 to 1:64 for serogroup C that have been correlated to the SBA-H protective titer. The serogroup W-135 assay at a SBA-BR titer of 1:64, has a specificity of 52%, but as the titer is increased to 1:128 and 1:256, specificity increases to 64 and 77%, respectively. As with serogroup Y, a threshold titer of >= 1:256 provides good assurance of of a protective titer in the human complement assay of 1:4 and 1:8. Like serogroup Y, sensitivity and specificity are better balanced at a threshold titer of 1:128 for serogroup W135. The range . of SBA-BR titers of 1:64 to 1:128 for serogroup W135 represent the equivocal range compared to the range of SBA-BR titers of 1:16 to 1:64 for serogroup C that are correlated to the SBA-H protective titer in this study. The four-fold rise in bactericidal titers are calculated for each serogroup and separately analyzed by vaccine group using both assays. In general, there is an indication that a higher four-fold rise in SBA titer (BR and H) is detected at higher post-immunization SBA-BR titers for all three serogroups. There are differences in the four-fold rises in SBA titers (BR vs. H) both by serogroup and by vaccine group. For serogroup C, four-fold rises in the assay with human complement appeared lower compared to titers in the assay with baby rabbit complement at low post-immunization SBA-BR titers. However at higher post-immunization SBA-BR titers, me four-fold rise in titer appeared higher in the assay with human complement. This pattern seems to suggest that at low post-immunization SBA-BR titers, the assay is less sensitive with human complement than it is with baby rabbit complement, but at high post-immunization SBA-BR titers, the opposite is true, that is, the assay with human complement becomes more sensitive. This pattern is not apparent when assaying samples from the polysaccharide vaccine group. In those samples the four-fold rise in titer appeared lower when using human complement in the assay. Although no explanation for this observation between sample type is apparent, it does suggest that the 146 assay performed with human complement lacks sensitivity with serum samples containing low titers of bactericidal activity. For serogroup Y, there is good agreement in the four-fold rises in SB A titers in comparing the two complement sources. The four-fold rises in SBA titers (BR and H) are slightly higher for the conjugate group compared to the polysaccharide group, but the difference is not as large as noted for serogroup C. For serogroup W135, the agreement between four-fold rise in SBA titers using human complement or baby rabbit complement in the assay for either vaccine group is not as good as compared to the results with the other two serogroup assays. The, four-fold rise by SBA-BR titer is very good for both vaccine groups, but the proportion of four-fold rise titers by SBA-H is lower compared to the other two serogroups. The four-fold rise by SBA-H in the polysaccharide groups is quite low, and comparatively lower in the four-fold rise in SBA-H titers for the other two serogroups. Four-fold rise in SBA titer using BR complement has been the benchmark for registration of the meningococcal polysaccharide vaccines. More recently, an effort has been made to link four-fold rise in SBA-BR titers to clinical efficacy from the post-registration surveillance data on the monovalent C conjugates in the United Kingdom (Borrow R, et al., 2001, Infect. Immun. 69:1568-1573). Based on this analysis the efficacy of the monovalent-C conjugates in toddlers, ranging in age from 12 to 30 months, has been estimated at 88% (69 to 95%) within 16 months of the first dose. For this age group, the proportion of subjects achieving a four-fold rise in SBA-BR titer ranges from 89 to 100% following one dose of the monovalent C conjugate vaccines. The SBA-BR provided herein provides bactericidal titer values that are comparable to the values obtained using human complement as the source of complement in the assay for serogroup C. Therefore, these SBA-BR titers are relevant to the original studies that established the surrogate for protective immunity to serogroup C meningococcal disease and support the extrapolation of the clinical results provided herein to protection, and the SBA-BR titers for serogroup C at are comparable to those reported from other laboratories. Performance of the SBA using human complement in the determination of the serogroup 147 specific response to serogroup Y and serogroup W-135 capsular polysaccharides, by analogy to the serogroup C model, support the relevance of the SBA-BR for determining bactericidal titers to serogroups Y and W-135. 148 We claim: 1. A polysaccharide-protein conjugate, wherein a conjugate comprises a capsular polysaccharide of N. meningitidis serogroup A, C, W-135orY, conjugated to one or more a carrier protein(s), and the composition comprises 0.5 to 15 gg/ml of each capsular polysaccharide to a average size of less than 100,000 daltons. 2. The conjugate according to claim 1, wherein the capsular polysaccharide is derivatized to average size of 5,00ft Id 75;000 daltons. 3. The conjugate according to claim 2, wherein the capsular polysaccharide is derivatized to average size of 7,000 to 50,000 daltons. 4. The conjugate according to claim 3, wherein the capsulu polysaccharide is derivatized to average size of 8000 to 35000 daltons. 5. The conjugate according to claim 4, wherein die capsular polysaccharide is derivatized to average size of 12,000 to 25,000 daltons. 20 6. The conjugate according to claim 5, wherein the capsular polysaccharide is derivatized to average size of 45,-0Q() to 22,000 daltons. 7. The conjugate according to claim 1, wherein the average ratio of derivatized polysaccharide to carrier protein is about 1:1 to about 1:20 (w/w). 8. The composition according to claim 7, wherein the average ratio of derivatized polysaccharide to carrier protein is about 1:2 to about 1:10 (w/w). 9. The composition according to claim 8, wherein the average ratio of derivatized 30 polysaccharide to carrier protein is about 1:2 to about 1:6 (w/w). 10. The composition according to claim 9, wherein the average ratio of derivatized polysaccharide to carrier protein is about 1 :(4±1) (w/w). 149 11. The composition according to claim 10, wherein the average ratio of derivatized polysaccharide to carrier protein is about 1 :(4±0.5) (w/w). 12.The composition according to claim 11, wherein the average ratio of derivatized polysaccharide to carrier protein is about 1 :(4±0.25) (w/w). 13. The conjugate according to claim 1, wherein the carrier protein comprises a bacterial toxin or toxoid, or a bacterial outer membrane protein, 14. The conjugate according to claim 1, wherein the carrier protein comprises a diphtheria toxin, diphtheria toxoid, CRM197, tetanus toxoid, pertussis toxoid, E. coli LT, E. coli ST, exotoxin A, outer membrane complex c (OMPC), porin, transferrin binding protein, pneumolysis, pneumococcal surface protein A(PspA ) pneumococcal aaesin protein (PsaA), ovalbumin, keyhole limpit hemocyanin (I~LH), bovine serum albumin (BSA) or purified protein derivative of tuberculin (PPD). 1S. The conjugate according to claim 14, wherein the carrier protein comprises a diphtheria toxin, diphtheria toxoid, CRM197, tetanus toxoid, exotoxin A, or outer membrane 20 complex C (OMPC). 16. The conjugate according to claim 15, wherein the carrier protein comprises a diphtheria toxin, diphtheria toxoid, or CRM197. 25 17. The conjugate according to claim 16, wherein the carrier protein comprises a diphtheria toxin, or diphtheria toxoid, 18. The conjugate according to claim 17, wherein the capsular polysaccharide is derivatized to average size of 8,000 to 35,000 daltons. 19. The conjugate according to claim 17, wherein the average ratio of derivatized polysaccharide to carrier protein is about 1:2 to about 1:10 (w/w). 150 20. The conjugate according to claim 19, wherein the average ratio of derivatized polysaccharide to carrier protein is about U(4±l) (w/v). 21. A composition comprising a polysaccharide-protein conjugate, wherein a conjugate comprises two or more capsular polysaccharides of N. meningitidis of serogroup A, C, W-135 or Y, conjugated to one or more a carrier protein(s), and the composition comprises 0.5 to 15 Hg/ml of each capsular polysaccharide to a average size of less than 100,000 daltons. 22. The composition according to claim 21, wherein the capsular polysaccharide is derivatized to average size of 5,000 to 75,000 daltons. 23. The composition according to claim 22, wherein the capsular polysaccharide is derivatized to average size of 7,000 to 50,000 daltons. 15 24. The composition according to claim 23, wherein the capsular polysaccharide is derivatized to average size of 8,000 to 35,000 daltons. 25. The composition according to claim 24, wherein the capsular polysaccharide is derivatized to average size of 12,000 to 25,000 daltons. 26. The composition according to claim 25, wherein the capsular polysaccharide is derivatized to average size of 15,000 to 22,000 daltons. 27. The composition according to claim 21, wherein the average ratio of each derivatized polysaccharide to carrier protein is about 1:1 to about 1:20 (w/w). 28. The composition according to claim 27, wherein the average ratio of each derivatized polysaccharide to carrier protein is about 1:2 to about!: 10 (w/w). 30 29.The composition according to claim 28, wherein the average ratio of each derivatized polysaccharide to carrier protein is about 1:2 to about 1:6 (w/w). 151 30. The composition, according to claim 29 wherein the average ration of each derivatized polysaccharide to carrier protein is about 1 :(4±1) (w/w). 31. The composition according to claim 30, wherein the average ratio of each derivatized polysaccharide to carrier protein is about 1:(4±0.5) (w/w). 32. The composition according to claim,31, wherein-.the average ratjo of each derivatized polysaccharide to carrier protein is about 1 :(4±0.25) (w/w). ...tit 10 33.The composition according to claim 31, wherein the composition is a liquid. 34. The composition according to claim 33, comprising about 0.5 to about 15 ug of N. meningococcal derivatized polysaccharide to serogroup A, C, W-135 or Y per milliliter of liquid. 35. The composition according to claim 33, comprising about 0.5 to about 15 ug of N. 15 meningococcal derivatized polysaccharide to serogroup W-135 or Y per milliliter of liquid. 36. The composition according to claim 31, wherein the carrier protein in diphtheria toxin or toxoid. 37. The composition according to claim 36, further comprising an adjuvant. 38. The composition according to claim 37, wherein the adjuvant comprises aluminum hydroxide, aluminum phosphate or combination thereof. 39. The composition according to claim 31, wherein the composition comprises sodium 25 phosphate, sodium chloride or combination thereof. 40. A method of immunizing a human patient against N. meningococcal disease by administration to the human patient a composition according to claims 21 to 39. 41. The method according to claim 40, Wherein the composition comprises an antigen to diphtheria, tetanus, pertussis FHA, pertussis PT, or PRP. 152 42. The method according to claim 40, wherein the composition according to. claim 21 is a first composition, and a second composition comprising an antigen to diphtheria, tetanus, pertussis FHA, pertussis PT, or PRP is administered to the human patient within six months of administration of the first composition. 43. The method according to claim 42, wherein the second composition comprising an antigen to diphtheria, tetanus, pertussis FHA, pertussis PT, or PRP is administered to the human patient within three months of administration of the first composition. 10 44. The method according to claim 43, wherein the second composition comprising an antigen to diphtheria, tetanus, pertussis FHA, pertussis PT, or PRP is administered to the human patient concomitantly with the administration of the first composition. 45. The method according to claim 40, wherein die human patjent is under the age of 60. 46. The method according to claim 45, wherein the human patient is between the ages of 35 and 60. 47. The method according to claim. 45, wherein the, human patient is between the ages of 20 60. 48. The method according to claim 45, wherein the human patient is between the ages of 18 and 35. "* 25 49. The method according to claim 45, wherein the human patient is between the ages of 18 and 25. 50. The method according to claim 45, wherein the human patient is between the ages of 15 and 18. 51. The method according to claim 45, wherein the human patient is between the ages of 10 and 15. 153 52. The method according to claim 45, wherein the human patient is under the age of 11. 53. The method according to claim 45, wherein the human patient is between the ages of 2 and 10. 54. The method according to claim 45, wherein the human patient under the age of 2. 55. The method according to claim 45, wherein the human patient is between the ages of 6 weeks and one year. 56. The composition according to claim 21, wherein the capsular polysaccharide is selected from the group consisting of A and W-135; Y and W-135, C and Y, C and W-135; A,CandY,A,CandW-135, (7) C,YandW-135, A,YandW-135 and.A,C,YandW-135 15 57. A method of inducing an immunological response against meningococcal A in a human patient, wherein the method comprises administering to the human patient a vaccine composition comprising a polysaccharide-protein conjugate, wherein the conjugate comprises a 0.5 to 15 ug/ml of capsular polysaccharide of N. meningitidis of serogroup A derivatized to an average size of less than 100,000 daltons. ..,,., 58. A method of inducing an immunological response against meningococcal C in a human patient, wherein the method comprises administering to the human patient a vaccine composition comprising a polysaccharide-protein conjugate, wherein the conjugate comprises a 0.5 to 15 ug/ml of capsular polysaccharide of N. meningitidis of serogroup C derivatized to an average size of less than 100,000 daltons. 59. A method of inducing an immunological response against meningococcal Y in a human patient, wherein the method comprises administering to the human patient a vaccine composition comprising a polysaccharide-protein conjugate, wherein the conjugate comprises a 0.5 to 15 ug/ml of capsular polysaccharide of N. meningitidis of serogroup Y derivatized to an average size of less than 100,000 daltons. 154 60. A method of inducing an immunological response against meningococcal W-135 in a human patient, wherein the method comprises administering to the human patient a vaccine composition comprising a polysaccharide-protein conjugate, wherein the conjugate comprises a 0.5 to 15 ug/ml of capsular polysaccharide of N. meningitidis of serogroup W- 135 derivatized to an average size of less than 100,000 daltons. 61. The method according to any of claims 57 to 60, wherein the vaccine composition does not comprise an adjuvant. 62. A method of immunizing a human patient against N. meningitidis by administration of a vaccine composition comprising a conjugate according to claims 1 to 20, whereby the human patient has a fourfold or-.greater increase in serum GMT or IgG titer within 28 d^s of vaccination compared with pre-administration serum GMT or IgG titer. ■ lit 63 .A method of immunizing a human patient against N. meningitidis by administration of a vaccine composition comprising a conjugate according to claims 1 to 20, whereby the human patient has a serum SBA-BR titer of 1:32 or higher within 20 to 40 days of vaccination compared with pre-administration SBA-BR titer. 64 .A method of immunizing a human patient against N. meningitidis by administration of a vaccine composition comprising a conjugate according to claims 1 to 20, whereby the human patient has a serum SBA-BR titer of 1:64 or higher within 20 to 40 days of vaccination compared with pre-administration SBA-BR titer. 65. A method of immunizing a human patient against N. meningitidis by administration of a vaccine composition comprising a conjugate according to claims"!" to 20, whereby the human patient has a serum SBA-BR titer of 1:128 or higher within 20 to 40 days of vaccination compared with pre-administration SBA-BR titer. 66. Multivalent meningococcal derivatized polysaccharide-protein conjugates and vaccineas herein described forgoing description and figures. Rajeshkumar H. Acharya Advocate & Patent Agent For and on Behalf of Applicant Dated this 23rd day of November 2005. 155 Abstract The present invention describes derivatized polysaccharide-protein conjugates, a composition comprising one or more of such derivatized polysaccharide-protein conjugates and methods of immunizing human patients with the same. The derivatized polysaccharide-protein conjugates are purified capsular polysaccharides from Neisseria meningitidis serogroups A, C, W-135, and Y, derivatized, chemically activated and selectively attached to a carrier protein by means of a covalent chemical bond, forming polysaccharide-protein conjugates capable of eliciting long-lasting immunity to a variety of N. meningitidis strains.

Documents:

1307-mumnp-2005-abstract(complete)-(24-11-2005).pdf

1307-mumnp-2005-abstract(granted)-(5-3-2008).pdf

1307-mumnp-2005-abstract.doc

1307-mumnp-2005-abstract.pdf

1307-mumnp-2005-cancelled pages(24-11-2005).pdf

1307-mumnp-2005-claims(amended)-(24-11-2005).pdf

1307-mumnp-2005-claims(complete)-(24-11-2005).pdf

1307-mumnp-2005-claims(granted)-(5-3-2008).pdf

1307-mumnp-2005-claims(marked copy)-(22-1-2008).pdf

1307-mumnp-2005-claims.doc

1307-mumnp-2005-claims.pdf

1307-mumnp-2005-correspondence(23-1-2008).pdf

1307-mumnp-2005-correspondence(ipo)-(25-2-2008).pdf

1307-mumnp-2005-correspondence-received-ver-100206.pdf

1307-mumnp-2005-correspondence-received-ver-140206.pdf

1307-mumnp-2005-correspondence-received-ver-221105.pdf

1307-mumnp-2005-descripiton (complete).pdf

1307-mumnp-2005-description(complete)-(24-11-2005).pdf

1307-mumnp-2005-description(granted)-(5-3-2008).pdf

1307-mumnp-2005-form 1(24-11-2005).pdf

1307-mumnp-2005-form 18(14-2-2006).pdf

1307-mumnp-2005-form 2(complete)-(24-11-2005).pdf

1307-mumnp-2005-form 2(granted)-(5-3-2008).pdf

1307-mumnp-2005-form 2(title page)-(complete)-(24-11-2005).pdf

1307-mumnp-2005-form 2(title page)-(granted)-(5-3-2008).pdf

1307-mumnp-2005-form 3(23-11-2005).pdf

1307-mumnp-2005-form 3(24-11-2005).pdf

1307-mumnp-2005-form-1.pdf

1307-mumnp-2005-form-2.doc

1307-mumnp-2005-form-2.pdf

1307-mumnp-2005-form-26.pdf

1307-mumnp-2005-form-5.pdf

1307-mumnp-2005-pct-search report.pdf

1307-mumnp-2005-wo internation publication report(23-1-2008).pdf