Study Phase 3

A Randomized, Double-blind Phase 3 Study to Assess the Immunogenicity and Safety of an Ad26.RSV.PreF-based Regimen at the End of Shelf-life in Adults Aged 60 to 75 Years

Trial Information

Generic NameAd26.RSV.preFProduct NameN/ATherapeutic AreaAnti-Infectives for Systemic UseProduct ClassVaccinesPharmacological SubgroupViral VaccinesChemical SubgroupOther Viral VaccinesCondition StudiedRespiratory Syncytial Viruses
Sponsor Protocol NumberVAC18193RSV3003Enrollment755Data PartnerJohnson & Johnson% Female55.3%Mean/Median Age (Years)65.6% White82.7%

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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