Ivacaftor (Kalydeco) and Insulin in Cystic Fibrosis (CF)
NCT02039986 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 13
Last updated 2018-12-14
Summary
This study is aimed at better understanding the impact of ivacaftor upon insulin and incretin secretion and glucose tolerance in patients with Cystic Fibrosis with a glycine (G551D) mutation. Investigators hypothesize that treatment with ivacaftor improves insulin secretion in individuals with CF.
Conditions
- Cystic Fibrosis Related Diabetes
- Cystic Fibrosis
Sponsors & Collaborators
-
Children's Hospital of Philadelphia
lead OTHER
Principal Investigators
-
Andrea Kelly, MD, MSCE · Children's Hospital of Philadelphia
Eligibility
- Min Age
- 6 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2014-01-06
- Primary Completion
- 2016-10-11
- Completion
- 2016-10-11
Countries
- United States
Study Locations
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