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The purpose of this study is to evaluate the safety, tolerability and efficacy of VX-121 combination therapy in subjects with cystic fibrosis (CF).
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Lead Sponsor
Vertex Pharmaceuticals Incorporated
NCT07102043 · Cystic Fibrosis Related Diabetes
NCT06616857 · Cystic Fibrosis (CF)
NCT05937815 · Cystic Fibrosis
NCT07148739 · Cystic Fibrosis (CF)
NCT02417740 · Cystic Fibrosis, Immunologic Deficiency Syndrome, and more
Keck Medical Center of University of Southern California
Los Angeles, California
Kaiser Permanente
Oakland, California
University of Kentucky.
Lexington, Kentucky
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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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