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A Phase 2a, Randomized, Double-blind, Placebo-controlled, Incomplete Block, Crossover Study to Evaluate the Safety and Efficacy of VX-371 in Subjects Aged 12 Years or Older With Cystic Fibrosis, Homozygous for the F508del-CFTR Mutation, and Being Treated With Orkambi

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A Phase 2a, Randomized, Double-blind, Placebo-controlled, Incomplete Block, Crossover Study to Evaluate the Safety and Efficacy of VX-371 in Subjects Aged 12 Years or Older With Cystic Fibrosis, Homozygous for the F508del-CFTR Mutation, and Being Treated With Orkambi

Status: Completed
Phase of Trial: Phase II

Latest Information Update: 06 Nov 2021

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At a glance

  • Drugs Idrevloride (Primary) ; Idrevloride (Primary) ; Ivacaftor/lumacaftor
  • Indications Cystic fibrosis
  • Focus Adverse reactions; Therapeutic Use
  • Sponsors Parion Sciences; Vertex Pharmaceuticals

    • Most Recent Events

    • 22 May 2019 Trial has been completed in UK.
    • 25 Oct 2017 Primary endpoint (Absolute change in percent predicted forced expiratory volume in 1 second (FEV1)) has not been met, according to a Vertex Pharmaceuticals media release.
    • 03 Oct 2017 Status changed from active, no longer recruiting to completed.

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