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Clinical Trial Summary

This study will evaluate the pharmacokinetics (PK), safety, tolerability, efficacy, and pharmacodynamic effect of VX-659, tezacaftor (TEZ), and ivacaftor (IVA) when dosed in triple combination (TC) in Cystic Fibrosis (CF) subjects with F/F or F/MF genotypes.

The study was discontinued after completion of Part A due to Sponsor's discretion.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT03633526
Study type Interventional
Source Vertex Pharmaceuticals Incorporated
Contact
Status Terminated
Phase Phase 3
Start date August 3, 2018
Completion date January 18, 2019

See also
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