CompletedPhase 3NCT01705145
Study of Ivacaftor in Cystic Fibrosis Subjects 2 Through 5 Years of Age With a CFTR Gating Mutation
Studying Cystic fibrosis
Last synced from ClinicalTrials.gov
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Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- Vertex Pharmaceuticals Incorporated
- Principal Investigator
- Margaret Rosenfeld, MDSeattle Children's Hospital
- Intervention
- Ivacaftor(drug)
- Enrollment
- 35 target
- Eligibility
- 2-5 years · All sexes
- Timeline
- 2013 – 2014
Study locations (20)
- Birmingham, Alabama, United States
- Aurora, Colorado, United States
- Atlanta, Georgia, United States
- Indianapolis, Indiana, United States
- Lexington, Kentucky, United States
- Boston, Massachusetts, United States
- Detroit, Michigan, United States
- Grand Rapids, Michigan, United States
- Minneapolis, Minnesota, United States
- Kansas City, Missouri, United States
- Omaha, Nebraska, United States
- Pittsburgh, Pennsylvania, United States
- Salt Lake City, Utah, United States
- Charlottesville, Virginia, United States
- Richmond, Virginia, United States
- +5 more locations on ClinicalTrials.gov
Collaborators
Cystic Fibrosis Foundation
Primary source
Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.
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