A Phase 3, Randomized, Multicenter, Observer-blinded, Noninferiority Study to Evaluate the Immunogenicity and Safety of a Quadrivalent Inactivated Influenza Virus Vaccine (Seqirus QIV) With a US-licensed Quadrivalent Inactivated Comparator Influenza Virus Vaccine (Comparator QIV) in a Pediatric Population 6 Months Through 59 Months of Age

Trial Profile

A Phase 3, Randomized, Multicenter, Observer-blinded, Noninferiority Study to Evaluate the Immunogenicity and Safety of a Quadrivalent Inactivated Influenza Virus Vaccine (Seqirus QIV) With a US-licensed Quadrivalent Inactivated Comparator Influenza Virus Vaccine (Comparator QIV) in a Pediatric Population 6 Months Through 59 Months of Age

Active, no longer recruiting
Phase of Trial: Phase III

Latest Information Update: 26 Jun 2017

At a glance

  • Drugs Influenza vaccine quadrivalent bioCSL (Primary)
  • Indications Influenza virus infections
  • Focus Pharmacodynamics
  • Sponsors Seqirus
  • Most Recent Events

    • 26 Jun 2017 Planned End Date changed from 1 May 2017 to 12 Aug 2017.
    • 24 Apr 2017 Status changed from recruiting to active, no longer recruiting.
    • 03 Oct 2016 Status changed from not yet recruiting to recruiting.
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