Safety and immunogenicity of a 15-valent pneumococcal conjugate vaccine in Japanese healthy infants: A Phase I study (V114-028)

This Phase I study evaluated the safety, tolerability, and immunogenicity of V114, a 15-valent pneumococcal conjugate vaccine (PCV), via subcutaneous (SC) or intramuscular (IM) administration, in healthy Japanese infants 3 months of age. A total of 133 participants were randomized to receive four do...

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Main Authors: Yasunori Ishihara (Author), Haruo Kuroki (Author), Hidenobu Hidaka (Author), Kazuyuki Iwai (Author), Keiko Wan (Author), Masayoshi Shirakawa (Author), Miyuki Sawata (Author)
Format: Book
Published: Taylor & Francis Group, 2023-01-01T00:00:00Z.
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100 1 0 |a Yasunori Ishihara  |e author 
700 1 0 |a Haruo Kuroki  |e author 
700 1 0 |a Hidenobu Hidaka  |e author 
700 1 0 |a Kazuyuki Iwai  |e author 
700 1 0 |a Keiko Wan  |e author 
700 1 0 |a Masayoshi Shirakawa  |e author 
700 1 0 |a Miyuki Sawata  |e author 
245 0 0 |a Safety and immunogenicity of a 15-valent pneumococcal conjugate vaccine in Japanese healthy infants: A Phase I study (V114-028) 
260 |b Taylor & Francis Group,   |c 2023-01-01T00:00:00Z. 
500 |a 2164-5515 
500 |a 2164-554X 
500 |a 10.1080/21645515.2023.2180973 
520 |a This Phase I study evaluated the safety, tolerability, and immunogenicity of V114, a 15-valent pneumococcal conjugate vaccine (PCV), via subcutaneous (SC) or intramuscular (IM) administration, in healthy Japanese infants 3 months of age. A total of 133 participants were randomized to receive four doses (3 + 1 regimen) of V114-SC (n = 44), V114-IM (n = 45), or 13-valent PCV (PCV13)-SC (n = 44) at 3, 4, 5, and 12-15 months of age. Diphtheria, tetanus, and pertussis-inactivated poliovirus (DTaP-IPV) vaccine was administered concomitantly at all vaccination visits. The primary objective was to assess the safety and tolerability of V114-SC and V114-IM. Secondary objectives were to assess the immunogenicity of PCV and DTaP-IPV at 1-month post-dose 3 (PD3). On days 1-14 following each vaccination, the proportions of participants with systemic adverse events (AEs) were comparable across interventions, whereas injection-site AEs were higher with V114-SC (100.0%) and PCV13-SC (100.0%) than with V114-IM (88.9%). Most AEs were mild or moderate in severity and no vaccine-related serious AEs or deaths were reported. Serotype-specific immunoglobulin G (IgG) response rates at 1-month PD3 were comparable across groups for most shared serotypes between V114 and PCV13. For additional V114 serotypes 22F and 33F, IgG response rates were higher with V114-SC and V114-IM than with PCV13-SC. DTaP-IPV antibody response rates at 1-month PD3 for V114-SC and V114-IM were comparable with PCV13-SC. Findings suggest that vaccination with V114-SC or V114-IM in healthy Japanese infants is generally well tolerated and immunogenic. 
546 |a EN 
690 |a clinical trial 
690 |a pcv15 
690 |a pcv13 
690 |a dtap-ipv 
690 |a pneumococcal infections 
690 |a pneumococcal vaccines 
690 |a japan 
690 |a child 
690 |a infant 
690 |a Immunologic diseases. Allergy 
690 |a RC581-607 
690 |a Therapeutics. Pharmacology 
690 |a RM1-950 
655 7 |a article  |2 local 
786 0 |n Human Vaccines & Immunotherapeutics, Vol 19, Iss 1 (2023) 
787 0 |n http://dx.doi.org/10.1080/21645515.2023.2180973 
787 0 |n https://doaj.org/toc/2164-5515 
787 0 |n https://doaj.org/toc/2164-554X 
856 4 1 |u https://doaj.org/article/bd2f6571c8134d74b33d486dc8c24bf6  |z Connect to this object online.