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A Phase IIIA Study of Immunogenicity and Safety of GSK Biologicals' Quadrivalent Split Virion Influenza Vaccine FLU-Q-QIV in Adults Aged 18 Years and Older

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Trial Profile

A Phase IIIA Study of Immunogenicity and Safety of GSK Biologicals' Quadrivalent Split Virion Influenza Vaccine FLU-Q-QIV in Adults Aged 18 Years and Older

Status: Completed
Phase of Trial: Phase III

Latest Information Update: 22 Aug 2023

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At a glance

  • Drugs GSK 2282512A (Primary)
  • Indications Influenza virus infections
  • Focus Pharmacodynamics
  • Sponsors GlaxoSmithKline; GSK

    • Most Recent Events

    • 21 Nov 2016 According to a GSK media release, based on the data from this and other three studies, the US FDA approved supplemental Biologics License Application for FluLaval Quadrivalent (Influenza Vaccine) for use in children of 6 months and older.
    • 04 Nov 2011 Status changed from active, no longer recruiting to completed as reported by ClinicalTrials.gov.
    • 14 Oct 2011 Status changed from not yet recruiting to active, no longer recruiting as reported by ClinicalTrials.gov.

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