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Study of the Effect of Ivacaftor on Lung Clearance Index in Subjects With Cystic Fibrosis and the G551D Mutation

Ivacaftor · Phase 2

Registry ID
NCT01262352
Phase
Phase 2
Status
Completed
Drug / intervention
Ivacaftor
Sponsor
Vertex Pharmaceuticals Incorporated
Start
2011-01
Enrollment
21
Locations
8

About this trial

The purpose of this study is to evaluate the effect of ivacaftor (VX-770) on lung clearance index (LCI) in subjects aged 6 years and older with cystic fibrosis (CF) who have the G551D-CFTR mutation on at least 1 allele.

View NCT01262352 on ClinicalTrials.gov →

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Medical disclaimer. This page summarizes public trial data for NCT01262352 for information only. It is not medical advice, an endorsement, or an offer to enroll. Confirm details on ClinicalTrials.gov and with a qualified physician.