VX17-659-103 Efficacy and Safety of VX-659/TEZ/IVA in CF Homozygous

  • Research type

    Research Study

  • Full title

    A Phase 3, Randomised, Double-blind, Controlled Study Evaluating the Efficacy and Safety of VX-659 Combination Therapy in Subjects With Cystic Fibrosis Who Are Homozygous for the F508del Mutation (F/F)

  • IRAS ID

    241640

  • Contact name

    Peter Barry

  • Contact email

    peter.barry@mft.nhs.uk

  • Sponsor organisation

    Vertex Pharmaceuticals Incorporated

  • Eudract number

    2017-004133-82

  • Clinicaltrials.gov Identifier

    NCT03447249

  • Duration of Study in the UK

    0 years, 7 months, 18 days

  • Research summary

    Cystic fibrosis (CF) is a chronic lifelong disease resulting from mutations in one gene called the cystic fibrosis transmembrane conductance regulator (CFTR) gene. Mutations in this CF-causing gene can affect the amount or the function of the protein made from this gene. VX-659, tezacaftor and ivacaftor are a triple combination of therapies targeted at improving the function of this protein. This triple combination has shown positive effects in some patients with CF.

    This clinical trial will evaluate if the triple combination will treat CF in men and women with CF who are 12 years of age or older, and who have two copies of the CF gene mutation F508del. The study plans to include approximately 100 participants globally, who will be assigned to either active treatment group (triple combination of VX-659, tezacaftor and ivacaftor) or a group receiving tezacaftor and ivacaftor only. Tezacaftor and ivacaftor is a combined therapy approved in the US for individuals with CF and certain genetic mutations. The total study duration is approximately 16 weeks: a 4 week screening period, followed by a 4 week “run-in” period in which all participants will be given tezacaftor and ivacaftor, followed by the 4 week treatment period where half of the participants are assigned to the active treatment group (triple combination of VX-659, tezacaftor and ivacaftor) and the other half to tezacaftor and ivacaftor alone, finishing with an additional 4 weeks of safety follow-up. The study will check if the triple combination can improve lung function and other measures of health in people with CF

  • REC name

    North East - Tyne & Wear South Research Ethics Committee

  • REC reference

    18/NE/0103

  • Date of REC Opinion

    2 May 2018

  • REC opinion

    Further Information Favourable Opinion