Study Phase 3

A Randomized, Double-blind, Placebo-controlled Phase 3 Study to Evaluate the Immunogenicity and Safety of Ad26.RSV.preF-based Vaccine and High-dose Seasonal Influenza Vaccine, With and Without Coadministration, in Adults Aged 65 Years and Older

Trial Information

Generic NameAd26.RSV.preFProduct NameN/ATherapeutic AreaInfectious Disease & VaccinesEnrollment777% Female55.9%% White86.8%
Product ClassImmunizationsSponsor Protocol NumberVAC18193RSV3005Data PartnerJohnson & JohnsonCondition StudiedRespiratory Syncytial VirusesMean/Median Age (Years)70.5

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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