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A Phase 3 Study To Assess The Persistence Of Hsba Response Up To 48 Months After Completion Of A Primary Series Of Bivalent Rlp2086, And The Safety, Tolerability, And Immunogenicity Of A Booster Dose Of Bivalent Rlp2086

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Trial Profile

A Phase 3 Study To Assess The Persistence Of Hsba Response Up To 48 Months After Completion Of A Primary Series Of Bivalent Rlp2086, And The Safety, Tolerability, And Immunogenicity Of A Booster Dose Of Bivalent Rlp2086

Status: Completed
Phase of Trial: Phase III

Latest Information Update: 22 Dec 2021

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At a glance

  • Drugs Meningococcal vaccine group B (Primary)
  • Indications Meningococcal group B infections
  • Focus Adverse reactions; Pharmacodynamics; Registrational
  • Sponsors Pfizer

Most Recent Events

  • 29 Jun 2021 Results published in the Vaccine
  • 12 Feb 2019 Interim Results(n=736) assessing Persistence and 4-year boosting of the bactericidal response elicited by two- and three-dose schedules of MenB-FHbp published in the Vaccine
  • 05 Feb 2018 Status changed from recruiting to completed.

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