A Phase II, randomized, immunogenicity and safety study of a quadrivalent meningococcal conjugate vaccine, MenACYW-TT, in healthy adolescents in the United States

被引:30
作者
Chang, Lee-Jah [1 ]
Hedrick, James [2 ]
Christensen, Shane [3 ]
Pan, Judy [1 ]
Jordanov, Emilia [1 ]
Dhingra, Mandeep S. [1 ]
机构
[1] Sanofi Pasteur, 1 Discovery Dr, Swiftwater, PA 18370 USA
[2] Kentucky Pediat Adult Res, Bardstown, KY USA
[3] J Lewis Res Inc, Salt Lake City, UT USA
关键词
MenACYW-TT; Invasive meningococcal disease; Meningococcal vaccine naive adolescents; Conjugate vaccine; HPV4; Tdap; Concomitant vaccine; DISEASE; INFECTION; INFANTS; RISK;
D O I
10.1016/j.vaccine.2020.03.017
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background: MenACYW-TT is an investigational quadrivalent meningococcal conjugate vaccine intended for use in individuals >= 6 weeks of age. We evaluated the safety and immunogenicity of MenACYW-TT when compared to a licensed quadrivalent conjugate meningococcal vaccine (Menveo (R); MCV4-CRM; GlaxoSmithKline, Italy), and when co-administered with tetanus, diphtheria, acellular pertussis (Tdap) and human papilloma virus (HPV4) vaccines in healthy meningococcal vaccine-naive adolescents (10-17 years old) in the United States of America. Methods: In this pivotal Phase II, open-label, multicenter study, 1715 participants were randomized to receive MenACYW-TT, MCV4-CRM, MenACYW-TT co-administered with Tdap and HPV4, or Tdap and HPV4 vaccines alone (NCT02199691). The primary objective was to evaluate whether antibody responses to MenACYW-TT antigens were non-inferior to antibody responses after MCV4-CRM administration. Meningococcal antibody titers were determined using human complement serum bactericidal assay (hSBA) with titers measured at baseline, and 30 days post vaccination (D30). A vaccine seroresponse was defined as baseline titers <1:8 with postvaccination titers >= 1:8 or baseline titers >= 1:8 with a >= 4-fold increase at post-vaccination. Safety data were collected up to six months post-vaccination. Results: Non-inferiority was demonstrated for MenACYW-TT vs MCV4-CRM (primary endpoint), and for MenACYW-TT co-administered with Tdap and HPV4 vs MenACYW-TT alone (secondary endpoint). The vaccine seroresponse rate was higher with MenACYW-TT than with MCV4-CRM, for each serogroup: A: 75.6% vs 66.4%; C: 97.2% vs 72.6%; W: 86.2% vs 66.6%; Y: 97.0% vs 80.8%. The safety profiles of MenACYW-TT, MCV4-CRM, and Tdap and HPV4 vaccines, administered with or without MenACYW-TT, were comparable. There were no vaccine-related serious adverse events. Conclusions: The MenACYW-TT vaccine was well tolerated and generated an immune response that was non-inferior to the licensed MCV4-CRM vaccine. Immunogenicity and safety profiles were comparable when MenACYW-TT was administered with or without Tdap and HPV4 vaccines in meningococcal vaccine-naive adolescents. (C) 2020 The Authors. Published by Elsevier Ltd.
引用
收藏
页码:3560 / 3569
页数:10
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