drugset / Trial / NCT03633526

Evaluation of VX-659/TEZ/IVA in Cystic Fibrosis Subjects 6 Through 11 Years of Age

NCT03633526

Phase 3 Terminated 18 enrolled Vertex Pharmaceuticals Incorporated
SequentialOpen-labelTreatment

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.

Timeline

Start
2018-08-03
Primary completion
2019-01-18
Completion
2019-01-18

Drugs

EvaluationDrugModalityDoseRoute
Subject BAMOCAFTOR Small molecule 120 mg
Subject Ivacaftor Other / unclassified 75 mg
Subject tezacaftor Other / unclassified 50 mg

Indications