drugset / Trial / NCT01931839

A Phase 3 Rollover Study of Lumacaftor in Combination With Ivacaftor in Subjects 12 Years and Older With Cystic Fibrosis

NCT01931839

Phase 3 Completed 1164 enrolled Vertex Pharmaceuticals Incorporated
RandomizedParallel-groupTriple-blindTreatment

Summary

The purpose of this study is to evaluate the efficacy and safety of long-term treatment with lumacaftor in combination with ivacaftor in people 12 years and older with Cystic Fibrosis.

Timeline

Start
2013-10
Primary completion
2016-04
Completion
2016-04

Drugs

EvaluationDrugModalityDoseRoute
Subject Ivacaftor Other / unclassified 250 mg Oral
Subject Lumacaftor Small molecule 400 mg Oral
Subject Lumacaftor Small molecule 600 mg Oral

Indications