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Clinical Trial Summary

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


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT06460506
Study type Interventional
Source Vertex Pharmaceuticals Incorporated
Contact Medical Information
Phone 617-341-6777
Email medicalinfo@vrtx.com
Status Not yet recruiting
Phase Phase 3
Start date October 2024
Completion date September 2027

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