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A Phase 3, Randomized, Multicenter, Double-blinded Study to Evaluate the Immunogenicity and Safety of a Quadrivalent Influenza Vaccine (CSL QIV) in Comparison With a US Licensed 2014/2015 Trivalent Influenza Vaccine (CSL TIV-1), and a Trivalent Influenza Vaccine Containing the Alternate B Strain (CSL TIV-2), in Adults Aged 18 Years and Above

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Trial Profile

A Phase 3, Randomized, Multicenter, Double-blinded Study to Evaluate the Immunogenicity and Safety of a Quadrivalent Influenza Vaccine (CSL QIV) in Comparison With a US Licensed 2014/2015 Trivalent Influenza Vaccine (CSL TIV-1), and a Trivalent Influenza Vaccine Containing the Alternate B Strain (CSL TIV-2), in Adults Aged 18 Years and Above

Status: Completed
Phase of Trial: Phase III

Latest Information Update: 16 Mar 2017

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At a glance

  • Drugs Influenza vaccine quadrivalent Seqirus (Primary) ; Influenza virus vaccine
  • Indications Influenza A virus infections; Influenza B virus infections
  • Focus Pharmacodynamics; Registrational
  • Sponsors CSL

    • Most Recent Events

    • 13 Mar 2017 Primary endpoint (The Seroconversion Rate (SCR) (Statistical Analysis: Difference in SCR) in Subjects Aged 18 Years.) has been met, according to the results published in the Vaccine
    • 13 Mar 2017 Primary endpoint (Postvaccination Geometric Mean Titer (GMT) (Statistical Analysis: GMT Ratios) in Subjects Aged 18 Years) has been met, according to the results published in the Vaccine
    • 13 Mar 2017 Results published in the Vaccine

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