drugset / Trial / NCT04058366

Study Evaluating the Long-term Safety and Efficacy of VX-445 Combination Therapy

NCT04058366

Phase 3 Completed 251 enrolled Vertex Pharmaceuticals Incorporated
NaSingle-groupOpen-labelTreatment

Summary

This study evaluated the long-term safety, efficacy, and pharmacodynamics of elexacaftor (ELX, VX-445) in triple combination (TC) with tezacaftor (TEZ) and ivacaftor (IVA) in subjects with cystic fibrosis (CF) who are heterozygous for the F508del mutation and a gating or residual function mutation (F/G and F/RF genotypes).

Timeline

Start
2019-12-05
Primary completion
2022-12-16
Completion
2022-12-16

Drugs

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

Indications