Science and Research

A Phase 3, Open-label Study Evaluating the Long-term Safety and Efficacy of VX-445 Combination Therapy in Subjects With Cystic Fibrosis Who Are Heterozygous for the F508del Mutation and a Gating or Residual Function Mutation (F/G and F/RF Genotypes) (VX18-445-110)

This study evaluated the long-term safety, efficacy, and pharmaco-dynamics of elexacaftor (ELX, VX-445) in triple combination (TC) with tezacaftor (TEZ) and ivacaftor (IVA) in subjects with cystic fibrosis (CF) who are heterozygous for the F508del mutation and a gating or residual function mutation (F/G and F/RF genotypes).

Study details
Study-ID: NCT04058366, 2019-000833-37
DZL Disease Area: CFBE
Study Type: Interventional
DZL Role: DZL recruiting center
Funding: Externally - industry
DZL Participating Sites: UGMLC
Start Date: 01.12.2019
Completion Date: 01.12.2022
Status: Closed
Link to Study


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