drugset / Trial / NCT04105972

A Study Evaluating the Efficacy and Safety of VX-445/Tezacaftor/Ivacaftor in Cystic Fibrosis Subjects, Homozygous for F508del

NCT04105972

Phase 3 Completed 176 enrolled Vertex Pharmaceuticals Incorporated
RandomizedParallel-groupQuadruple-blindTreatment

Summary

This study will evaluate the efficacy, safety, 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 homozygous for F508del.

Timeline

Start
2019-10-03
Primary completion
2020-07-24
Completion
2020-07-24

Drugs

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

Indications