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Clinical Trial Summary

This study will evaluate the long-term safety and tolerability of VX-445 in triple combination (TC) with tezacaftor (TEZ) and ivacaftor (IVA) in subjects with cystic fibrosis (CF) who are homozygous or heterozygous for the F508del mutation


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT03525574
Study type Interventional
Source Vertex Pharmaceuticals Incorporated
Contact
Status Completed
Phase Phase 3
Start date October 9, 2018
Completion date January 9, 2023

See also
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