Study Phase 1

A Randomized, Double-blind, Placebo-controlled, Phase 1 Study to Evaluate the Safety, Reactogenicity and Immunogenicity of Single Vaccination of an Ad26.RSV.preF-based Regimen in Japanese Adults Aged 60 Years and Older

Trial Information

Generic NameAd26.RSV.preFProduct NameN/ATherapeutic AreaAnti-Infectives for Systemic UseProduct ClassVaccinesCondition StudiedRespiratory Syncytial VirusesChemical SubgroupsN/APharmacological SubgroupsN/A
Sponsor Protocol NumberVAC18193RSV1006Enrollment36Data PartnerJohnson & Johnson% Female44.4%Mean/Median Age (Years)65.7% White0.0%

Supporting Documentation

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

Disclaimer

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