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Clinical Trial Summary

The purpose of this study is to evaluate the pharmacokinetics, safety, tolerability and efficacy of VX-121/tezacaftor/deutivacaftor (VX-121/TEZ/D-IVA) in CF participants with at least 1 triple combination responsive (TCR) mutation in the cystic fibrosis transmembrane conductance regulator (CFTR) gene.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05422222
Study type Interventional
Source Vertex Pharmaceuticals Incorporated
Contact
Status Active, not recruiting
Phase Phase 3
Start date June 21, 2022
Completion date June 2030

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