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A Randomized, Double-blind, Placebo-controlled Phase 1/2a Study for Safety and Immunogenicity Evaluations for Regimen Selection of Ad26.RSV.preF and/or RSV preF Protein Combinations Followed by Expanded Safety Evaluation in Adults Aged 60 Years and Older

Trial Profile

A Randomized, Double-blind, Placebo-controlled Phase 1/2a Study for Safety and Immunogenicity Evaluations for Regimen Selection of Ad26.RSV.preF and/or RSV preF Protein Combinations Followed by Expanded Safety Evaluation in Adults Aged 60 Years and Older

Status: Completed
Phase of Trial: Phase I/II

Latest Information Update: 15 Sep 2023

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At a glance

  • Drugs JNJ 64400141 (Primary) ; JNJ-64213175 (Primary)
  • Indications Respiratory syncytial virus infections
  • Focus Adverse reactions; Pharmacodynamics
  • Sponsors Janssen Vaccines and Prevention B.V
  • Most Recent Events

    • 11 Jul 2023 Results assessing safety immunogenicity and regimen selection of Ad26.RSV.preF-based Vaccine published in the Journal of Infectious Diseases
    • 02 Aug 2022 Status changed from active, no longer recruiting to completed.
    • 19 Feb 2021 Planned primary completion date changed from 30 Apr 2021 to 30 May 2022.
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