Study Phase 3

A Randomized, Double-blind Phase 3 Study to Compare the Immunogenicity of Clinical Trial Material of an Ad26.RSV.preF-based Vaccine for Phase 3 With Clinical Trial Material Representative of Phase 2b in Adults Aged 60 to 75 Years

Trial Information

Generic NameAd26.RSV.preFProduct NameN/ATherapeutic AreaAnti-Infectives for Systemic UseProduct ClassVaccinesCondition StudiedRespiratory Syncytial VirusesChemical SubgroupsN/APharmacological SubgroupsN/A
Sponsor Protocol NumberVAC18193RSV3004Enrollment250Data PartnerJohnson & Johnson% Female51.6%Mean/Median Age (Years)64% White88.7%

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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