Science and Research

A Phase 3, Open-label Study Evaluating the Pharmacokinetics, Safety, and Tolerability of Elexacaftor/Tezacaftor/Ivacaftor in Cystic Fibrosis Subjects 12 to Less Than 24 Months of Age

This study will evaluate the pharmacokinetics (PK), safety, tolerability, pharmacodynamics (PD), and efficacy of ELX/TEZ/IVA in CF subjects 12 to less than (<) 24 months of age. To evaluate the safety and tolerability of ELX/TEZ/IVA

Study details
Study-ID: NCT05882357, 2023-503230-49-00
Study-ID: NCT05882357, 2023-503230-49-00
DZL Disease Area: CFBE
DZL Disease Area: CFBE
Study Type: Interventional
Study Type: Interventional
DZL Role: DZL recruiting center, DZL on steering board
DZL Role: DZL recruiting center, DZL on steering board
Funding: Externally - industry
Funding: Externally - industry
DZL Participating Sites: BIH / Charité - Associated Partner, BREATH
DZL Participating Sites: BIH / Charité - Associated Partner, BREATH
Start Date: 05.02.2024
Completion Date: 31.10.2025
Status: Closed
Status: Closed
DZL recruiting center, DZL on steering board
Link to Study


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