drugset / Trial / NCT02875366

A Study of the Effects of Lumacaftor/Ivacaftor (LUM/IVA) on Exercise Tolerance in Subjects With Cystic Fibrosis (CF), Homozygous for the F508del-CFTR Mutation

NCT02875366 ↗

Phase 4 Completed 70 enrolled Vertex Pharmaceuticals Incorporated
RandomizedParallel-groupTriple-blindOther

Summary

This is a Phase 4, randomized, double-blind, placebo-controlled, parallel-group study in subjects aged 12 years and older with CF who are homozygous for the F508del-CFTR mutation. This study is designed to evaluate the effect of LUM/IVA on exercise tolerance in subjects with CF, homozygous for the F508del-CFTR mutation.

Timeline

Start
2016-09
Primary completion
2017-09
Completion
2017-10

Outcome

Missed primary endpoint

paper The least-squares mean difference for lumacaftor/ivacaftor versus placebo in relative change in VO2max from baseline at Week 24 was -3.2% (95% CI: -9.2, 2.9; P=0.3021); PMID 33358691 ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject Ivacaftor Other / unclassified 250 mg Oral
Subject Lumacaftor Small molecule 400 mg Oral

Indications