Science and Research

A Phase 3, Open-label Study Evaluating the Long-term Safety and Efficacy of Elexacaftor/Tezacaftor/Ivacaftor in Cystic Fibrosis Subjects 12 Months of Age and Older

The purpose of the study is to evaluate the long-term safety, tolerability, efficacy, and pharmacodynamics (PD) of elexacaftor (ELX)/tezacaftor (TEZ)/ivacaftor (IVA).

Study details
Study-ID: NCT06460506, 2023-509563-24-00
Study-ID: NCT06460506, 2023-509563-24-00
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, BIH / Charité - Associated Partner
DZL Participating Sites: BREATH, BIH / Charité - Associated Partner
Start Date: 12.11.2024
Completion Date: 30.09.2027
Status: Active / not recruiting
Status: Active / not recruiting
DZL recruiting center
Link to Study


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