Study Phase 1, 2

A Randomized, Double-blind, Placebo-controlled Phase 1/2a Study for Safety and Immunogenicity Evaluations for Regimen Selection of Ad26.RSV.preF and/or RSV preF Protein Combinations Followed by Expanded Safety Evaluation in Adults Aged 60 Years and Older

Trial Information

Generic NameAd26.RSV.preFProduct NameN/ATherapeutic AreaInfectious Disease & VaccinesEnrollment669% Female60.0%% White87.2%
Product ClassImmunizationsSponsor Protocol NumberVAC18193RSV1004Data PartnerJohnson & JohnsonCondition StudiedRespiratory Syncytial VirusesMean/Median Age (Years)68.3

Supporting Documentation

  • Collected Datasets Available
  • Data Definition Specification Available
  • Protocol with Amendments Available
  • Statistical Analysis Plan Available
  • Clinical Study Report Available

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