Study Phase 2

A Randomized, Double-blind, Placebo-controlled Phase 2a Study to Evaluate the Safety and Immunogenicity of Seasonal Influenza Vaccine and Ad26.RSV.preF, With and Without Co-administration, in Adults Aged 60 Years and Older in Stable Health

Trial Information

Generic NameAd26.RSV.preFProduct NameN/ATherapeutic AreaAnti-Infectives for Systemic UseProduct ClassVaccinesCondition StudiedRespiratory Syncytial VirusesChemical SubgroupsN/APharmacological SubgroupsN/A
Sponsor Protocol NumberVAC18193RSV2003Enrollment180Data PartnerJohnson & Johnson% Female62.8%Mean/Median Age (Years)65% White88.9%

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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