Science and Research

A Phase 3, open-label, rollover study to evaluate the safety and efficacy of long-term treatment with tezacaftor in combination with ivacaftor in subjects with cystic fibrosis aged 6 years and old-er, homozygous or heterozygous for the F508del-CFTR mutation (VX17-661-116)

This study evaluates the long-term safety and tolerability of te-zacaftor in combination with ivacaftor (TEZ/IVA) in participants with cystic fibrosis (CF) aged 6 years and older, homozygous or heterozy-gous for the F508del mutation.

Study details
Study-ID: NCT03537651, 2017-002968-40
Study-ID: NCT03537651, 2017-002968-40
DZL Disease Area: CFBE
DZL Disease Area: CFBE
Study Type: Interventional
Study Type: Interventional
DZL Role: DZL recruiting center
DZL Role: DZL recruiting center
Funding: Externally - industry
Funding: Externally - industry
DZL Participating Sites: BREATH, UGMLC
DZL Participating Sites: BREATH, UGMLC
Start Date: 01.04.2018
Completion Date: 01.09.2023
Status: Closed
Status: Closed
DZL recruiting center
Link to Study


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