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A phase 3, multicenter,randomized, double-blind study to evaluate the interchangeability of V114, a 15-valent pneumococcal conjugate vaccine,and PCV13 with respect to safety,tolerability, and immunogenicity in healthy infants (PNEU-DIRECTION)
Institution:1. Merck & Co., Inc., Rahway, NJ, USA;2. Parkside Clinical Research and Tribe Clinical Research, Greenville, SC, USA;3. Clinical Research of Puerto Rico, Guayama, Puerto Rico;4. Mahidol University, Bangkok, Thailand;5. Chiang Mai University, Chiang Mai, Thailand;6. Khon Kaen University, Khon Kaen, Thailand;7. The Shraga Segal Dept. of Microbiology, Immunology and Genetics, Faculty of Health Sciences of the Ben-Gurion University of the Negev Beer-Sheva, Israel;8. University of Western Australia School of Medicine, Perth, Australia;9. MSD, China
Abstract:BackgroundPneumococcal disease (PD) remains a major health concern globally. In children, pneumococcal conjugate vaccines (PCVs) provide protection against PD from most vaccine serotypes, but non-vaccine serotypes contribute to residual disease. V114 is a 15-valent PCV containing all 13 serotypes in Prevnar 13? (PCV13) and public health important serotypes 22F and 33F. This phase 3 study evaluated safety and immunogenicity of mixed PCV13/V114 regimens using a 3 + 1 dosing schedule when changing from PCV13 to V114 at doses 2, 3, or 4.Methods900 healthy infants were randomized equally to 5 intervention groups. PCVs were administered in a 3-dose infant series at 2, 4, and 6 months of age followed by a toddler dose at 12–15 months along with concomitant routine vaccines. Safety was evaluated as the proportion of participants with adverse events (AEs). Immunoglobulin G (IgG) responses to the 15 serotypes in V114 were measured at 30 days post-dose 3 and 30 days post-dose 4 (PD4).ResultsFrequencies of injection-site and systemic AEs were generally comparable across all intervention groups. At 30 days PD4 (primary endpoint), IgG geometric mean concentrations (GMCs) for the 13 shared serotypes were generally comparable between mixed V114/PCV13 and 4-dose regimens of PCV13 or V114. In mixed regimens at 30 days PD4, a toddler dose of V114 was sufficient to achieve IgG GMCs comparable to a 4-dose regimen of V114 for serotype 22F, while at least one infant dose was needed in addition to the toddler dose to achieve IgG GMCs comparable to a 4-dose regimen of V114 for serotype 33F.ConclusionsV114 was well tolerated with a generally comparable safety profile to PCV13. For 13 shared serotypes, both mixed regimens and the V114 4-dose regimen induced generally comparable antibody responses to 4-dose regimen with PCV13. Study results support interchangeability of V114 with PCV13 in infants.Trial registration: ClinicalTrials.gov: NCT03620162; EudraCT: 2018–001151-12.
Keywords:Pneumococcal vaccine  Immunogenicity  Safety  Pediatric
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