A phase III, multicenter, randomized, double-blind, active comparator-controlled study to evaluate the safety, tolerability, and immunogenicity of catch-up vaccination regimens of V114, a 15-valent pneumococcal conjugate vaccine, in healthy infants, children, and adolescents (PNEU-PLAN)

dc.contributor.authorBanniettis N.
dc.contributor.authorWysocki J.
dc.contributor.authorSzenborn L.
dc.contributor.authorPhongsamart W.
dc.contributor.authorPitisuttithum P.
dc.contributor.authorRämet M.
dc.contributor.authorRichmond P.
dc.contributor.authorShi Y.
dc.contributor.authorDagan R.
dc.contributor.authorGood L.
dc.contributor.authorPapa M.
dc.contributor.authorLupinacci R.
dc.contributor.authorMcFetridge R.
dc.contributor.authorTamms G.
dc.contributor.authorChurchill C.
dc.contributor.authorMusey L.
dc.contributor.authorBickham K.
dc.contributor.otherMahidol University
dc.date.accessioned2023-06-18T16:44:39Z
dc.date.available2023-06-18T16:44:39Z
dc.date.issued2022-10-19
dc.description.abstractBackground: Despite widespread use of pneumococcal conjugate vaccines (PCVs) in children, morbidity and mortality caused by pneumococcal disease (PD) remain high. In addition, many children do not complete their PCV course on schedule. V114 is a 15-valent PCV that contains two epidemiologically important serotypes, 22F and 33F, in addition to the 13 serotypes present in PCV13, the licensed 13-valent PCV. Methods: This phase III descriptive study evaluated safety and immunogenicity of catch-up vaccination with V114 or PCV13 in healthy children 7 months–17 years of age who were either pneumococcal vaccine-naïve or previously immunized with lower valency PCVs (NCT03885934). Overall, 606 healthy children were randomized to receive V114 (n = 303) or PCV13 (n = 303) via age-appropriate catch-up vaccination schedules in three age cohorts (7–11 months, 12–23 months, or 2–17 years). Results: Similar proportions of children 7–11 months and 2–17 years of age reported adverse events (AEs) in the V114 and PCV13 groups. A numerically greater proportion of children 12–23 months of age reported AEs in the V114 group (79.0%) than the PCV13 group (59.4%). The proportions of children who reported serious AEs varied between different age cohorts but were generally comparable between vaccination groups. No vaccine-related serious AEs were reported, and no deaths occurred. At 30 days after the last PCV dose, serotype-specific immunoglobulin G geometric mean concentrations were comparable between vaccination groups for the 13 shared serotypes and higher in the V114 group for 22F and 33F. Conclusions: Catch-up vaccination with V114 in healthy individuals 7 months–17 years of age was generally well tolerated and immunogenic for all 15 serotypes, including those not contained in PCV13, regardless of prior pneumococcal vaccination. These results support V114 catch-up vaccination in children with incomplete or no PCV immunization per the recommended schedule.
dc.identifier.citationVaccine Vol.40 No.44 (2022) , 6315-6325
dc.identifier.doi10.1016/j.vaccine.2022.09.003
dc.identifier.eissn18732518
dc.identifier.issn0264410X
dc.identifier.pmid36150974
dc.identifier.scopus2-s2.0-85138564402
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/20.500.14594/83578
dc.rights.holderSCOPUS
dc.subjectBiochemistry, Genetics and Molecular Biology
dc.titleA phase III, multicenter, randomized, double-blind, active comparator-controlled study to evaluate the safety, tolerability, and immunogenicity of catch-up vaccination regimens of V114, a 15-valent pneumococcal conjugate vaccine, in healthy infants, children, and adolescents (PNEU-PLAN)
dc.typeArticle
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85138564402&origin=inward
oaire.citation.endPage6325
oaire.citation.issue44
oaire.citation.startPage6315
oaire.citation.titleVaccine
oaire.citation.volume40
oairecerif.author.affiliationSiriraj Hospital
oairecerif.author.affiliationFaculty of Tropical Medicine, Mahidol University
oairecerif.author.affiliationPoznan University of Medical Sciences
oairecerif.author.affiliationThe University of Western Australia
oairecerif.author.affiliationBen-Gurion University of the Negev
oairecerif.author.affiliationTampere University
oairecerif.author.affiliationMerck & Co., Inc.
oairecerif.author.affiliationWroclaw Medical University

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