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A Phase 3, Open-label, Randomized, Controlled, Multi-country Study to Evaluate the Immune Response, Safety and Reactogenicity of RSVPreF3 OA Investigational Vaccine When Co-administered With FLU-QIV Vaccine in Adults Aged 60 Years and Above

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A Phase 3, Open-label, Randomized, Controlled, Multi-country Study to Evaluate the Immune Response, Safety and Reactogenicity of RSVPreF3 OA Investigational Vaccine When Co-administered With FLU-QIV Vaccine in Adults Aged 60 Years and Above

Status: Completed
Phase of Trial: Phase III

Latest Information Update: 06 Sep 2024

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At a glance

  • Drugs Respiratory syncytial virus vaccine adjuvanted (Primary) ; Influenza virus vaccine
  • Indications Respiratory syncytial virus infections
  • Focus Pharmacodynamics; Registrational
  • Sponsors GlaxoSmithKline; GSK

    • Most Recent Events

    • 08 Jan 2024 Results evaluating the immunogenicity, reactogenicity, and safety of the AS01E-adjuvanted RSV prefusion F protein-based candidate vaccine (RSVPreF3 OA) when co-administered with a seasonal quadrivalent influenza vaccine (FLU-QIV) in older adults, published in the Clinical Infectious Diseases
    • 07 Apr 2022 Status changed from active, no longer recruiting to completed.
    • 17 Sep 2021 Planned primary completion date changed from 21 Sep 2021 to 29 Sep 2021.

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