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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Taylor & Francis Group,
2023-01-01T00:00:00Z.
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LEADER | 00000 am a22000003u 4500 | ||
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001 | doaj_bd2f6571c8134d74b33d486dc8c24bf6 | ||
042 | |a dc | ||
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. |