drugset / Trial / NCT03691779

Evaluation of VX 445/TEZ/IVA in Cystic Fibrosis Subjects 6 Through 11 Years of Age

NCT03691779

Phase 3 Completed 71 enrolled Vertex Pharmaceuticals Incorporated
Non-randomizedSequentialOpen-labelTreatment

Summary

This study will evaluate the pharmacokinetics (PK), safety, tolerability, efficacy, and pharmacodynamic effect of VX-445, tezacaftor (TEZ), and ivacaftor (IVA) when dosed in triple combination (TC) in Cystic Fibrosis (CF) subjects 6 through 11 years of age with F/F and F/MF genotypes.

Timeline

Start
2018-10-02
Primary completion
2020-08-07
Completion
2020-08-07

Drugs

EvaluationDrugModalityDoseRoute
Subject Ivacaftor Other / unclassified 75 mg Oral
Subject Ivacaftor Other / unclassified 150 mg Oral
Subject elexacaftor Small molecule 100 mg Oral
Subject elexacaftor Small molecule 200 mg Oral
Subject tezacaftor Other / unclassified 50 mg Oral
Subject tezacaftor Other / unclassified 100 mg Oral

Indications