A Phase 3, Randomized, Multicenter, Observer-Blinded, Noninferiority Study to Evaluate the Immunogenicity and Safety of a Seqirus Quadrivalent Inactivated Influenza Virus Vaccine (Seqirus QIV) With a US-Licensed 2015-2016 Quadrivalent Inactivated Comparator Influenza Vaccine (Comparator QIV) in a Pediatric Population 5 Through 17 Years of Age

Trial Profile

A Phase 3, Randomized, Multicenter, Observer-Blinded, Noninferiority Study to Evaluate the Immunogenicity and Safety of a Seqirus Quadrivalent Inactivated Influenza Virus Vaccine (Seqirus QIV) With a US-Licensed 2015-2016 Quadrivalent Inactivated Comparator Influenza Vaccine (Comparator QIV) in a Pediatric Population 5 Through 17 Years of Age

Completed
Phase of Trial: Phase III

Latest Information Update: 20 Apr 2017

At a glance

  • Drugs Influenza vaccine quadrivalent Seqirus (Primary) ; GSK 2321138A
  • Indications Influenza virus infections
  • Focus Pharmacodynamics; Registrational
  • Sponsors bioCSL; Seqirus
  • Most Recent Events

    • 05 Apr 2017 Results published in the Vaccine
    • 13 Jul 2016 Status changed from active, no longer recruiting to completed.
    • 14 Jan 2016 Planned End Date changed from 1 May 2016 to 1 Jul 2016 as per ClinicalTrials.gov record.
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