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1.
Int J Infect Dis ; 14(10): e868-75, 2010 Oct.
Article in English | MEDLINE | ID: mdl-20655261

ABSTRACT

BACKGROUND: This study compared the investigational quadrivalent meningococcal CRM197 conjugate vaccine, MenACWY-CRM, with licensed quadrivalent polysaccharide (MPSV4) and conjugate (MenACWY-D) meningococcal vaccines. METHODS: In this phase III multicenter study, 2505 adults (aged 19-55 years) were randomized to receive either MenACWY-CRM or MenACWY-D, and 326 adults (aged 56-65 years) were randomized to receive either MenACWY-CRM or MPSV4. Sera obtained pre-vaccination and at 1-month post-vaccination were tested for serogroup-specific serum bactericidal activity using human complement (hSBA) for immunogenicity non-inferiority and superiority analyses. RESULTS: The vaccines in all groups were well tolerated. In the 19-55 years age group, post-vaccination geometric mean titers (GMTs) were consistently higher for MenACWY-CRM than for MenACWY-D for all four serogroups. MenACWY-CRM was non-inferior to MenACWY-D for all serogroups, and superior for serogroup Y. In the 56-65 years age group, post-vaccination GMTs were 1.2- to 5.4-fold higher for MenACWY-CRM than for MPSV4 for the four serogroups. CONCLUSIONS: MenACWY-CRM is well tolerated and immunogenic in adults aged 19-65 years, with at least non-inferior immunogenicity compared with the currently licensed meningococcal vaccines.


Subject(s)
Meningococcal Vaccines/adverse effects , Meningococcal Vaccines/immunology , Vaccines, Conjugate/adverse effects , Vaccines, Conjugate/immunology , Adult , Argentina , Colombia , Female , Humans , Male , Middle Aged
2.
Vaccine ; 28(18): 3171-9, 2010 Apr 19.
Article in English | MEDLINE | ID: mdl-20189491

ABSTRACT

This Phase III study evaluates an investigational quadrivalent meningococcal CRM(197) conjugate vaccine, MenACWY-CRM (Novartis Vaccines), when administered concomitantly or sequentially with two other recommended adolescent vaccines; combined tetanus, reduced diphtheria and acellular pertussis (Tdap), and human papillomavirus (HPV) vaccine. In this single-centre study, 1620 subjects 11-18 years of age, were randomized to three groups (1:1:1) to receive MenACWY-CRM concomitantly or sequentially with Tdap and HPV. Meningococcal serogroup-specific serum bactericidal assay using human complement (hSBA), and antibodies to Tdap antigens and HPV virus-like particles were determined before and 1 month after study vaccinations. Proportions of subjects with hSBA titres > or =1:8 for all four meningococcal serogroups (A, C, W-135, Y) were non-inferior for both concomitant and sequential administration. Immune responses to Tdap and HPV antigens were comparable when these vaccines were given alone or concomitantly with MenACWY-CRM. All vaccines were well tolerated; concomitant or sequential administration did not increase reactogenicity. MenACWY-CRM was well tolerated and immunogenic in subjects 11-18 years of age, with comparable immune responses to the four serogroups when given alone or concomitantly with Tdap or HPV antigens. This is the first demonstration that these currently recommended adolescent vaccines could be administered concomitantly without causing increased reactogenicity.


Subject(s)
Adjuvants, Immunologic/adverse effects , Bacterial Proteins/adverse effects , Diphtheria-Tetanus-acellular Pertussis Vaccines/administration & dosage , Immunization/methods , Meningococcal Vaccines/adverse effects , Meningococcal Vaccines/immunology , Papillomavirus Vaccines/administration & dosage , Adjuvants, Immunologic/administration & dosage , Adolescent , Antibodies, Bacterial/blood , Antibodies, Viral/blood , Bacterial Proteins/administration & dosage , Blood Bactericidal Activity , Child , Drug-Related Side Effects and Adverse Reactions/epidemiology , Female , Humans , Immunization Schedule , Incidence , Male , Vaccines, Conjugate/adverse effects , Vaccines, Conjugate/immunology
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