Clinical Trials Directory

Trials / Completed

CompletedNCT01614457

Study of Ivacaftor in Subjects With Cystic Fibrosis (CF) Who Have the R117H-CF Transmembrane Conductance Regulator (CFTR) Mutation (KONDUCT)

A Phase 3, Randomized, Double-Blind, Placebo-Controlled, Parallel-Group Study to Evaluate the Efficacy and Safety of Ivacaftor in Subjects With Cystic Fibrosis Who Have the R117H-CFTR Mutation

Status
Completed
Phase
Phase 3
Study type
Interventional
Enrollment
70 (actual)
Sponsor
Vertex Pharmaceuticals Incorporated · Industry
Sex
All
Age
6 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study is to evaluate the efficacy and safety of ivacaftor in subjects with cystic fibrosis (CF) who have the R117H-CFTR mutation.

Detailed description

Ivacaftor is the first CFTR modulator to show an improvement in CFTR function and clinical benefit in subjects with CF. Results from Phase 3 studies (VX08-770-102 \[Study 102\] \[NCT00909532\] and VX08-770-103 \[Study 103\] \[NCT00909727\]) showed that ivacaftor is effective in the treatment of subjects with CF who have the G551D-CFTR mutation, as evidenced by sustained improvements in CFTR channel function (measured by reduction in sweat chloride concentration) and corresponding substantial, durable improvements in lung function, pulmonary exacerbations, respiratory symptoms, and weight gain. Ivacaftor was also well tolerated, as evidenced by the rates and reasons for premature discontinuation and results of safety assessments. Ivacaftor (Trade Name Kalydeco; 150 mg tablets) was initially approved in the United States for the treatment of CF in subjects 6 years of age and older who have a G551D mutation in the CFTR gene.

Conditions

Interventions

TypeNameDescription
DRUGIvacaftorIvacaftor 150 milligram (mg) tablet orally twice daily for 24 weeks.
DRUGPlaceboPlacebo matched to Ivacaftor tablet orally twice daily for 24 weeks.

Timeline

Start date
2012-07-01
Primary completion
2013-10-01
Completion
2013-10-01
First posted
2012-06-08
Last updated
2015-02-12
Results posted
2015-02-12

Locations

31 sites across 2 countries: United States, United Kingdom

Source: ClinicalTrials.gov record NCT01614457. Inclusion in this directory is not an endorsement.