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A Phase 2, Multicenter, Double-Blinded, Placebo Controlled Study to Evaluate Safety, Efficacy, Pharmacokinetics, and Pharmacodynamics of VX-661 Monotherapy and VX-661/Ivacaftor Cotherapy in Subjects With Cystic Fibrosis, Homozygous or Heterozygous for the F508del-CFTR Mutation
Conditions
Interventions
VX-661
Ivacaftor
+2 more
Locations
36
United States
Vertex Investigational Site
Birmingham, Alabama, United States
Vertex Investigational Site
Oakland, California, United States
Vertex Investigational Site
Boise, Idaho, United States
Vertex Investigational Site
Chicago, Illinois, United States
Vertex Investigational Site
Boston, Massachusetts, United States
Vertex Investigational Site
Grand Rapids, Michigan, United States
Start Date
February 1, 2012
Primary Completion Date
March 1, 2014
Completion Date
March 1, 2014
Last Updated
April 13, 2018
NCT02417740
NCT06616857
NCT02740868
NCT07108153
NCT07303621
NCT07274631
Lead Sponsor
Vertex Pharmaceuticals Incorporated
Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
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