Effect of Exendin-(9-39) on Fasting Adaptation and Protein Sensitivity
Status: | Completed |
---|---|
Conditions: | Endocrine |
Therapuetic Areas: | Endocrinology |
Healthy: | No |
Age Range: | Any - 18 |
Updated: | 1/20/2018 |
Start Date: | May 2009 |
End Date: | January 2017 |
Role of GLP-1 in Congenital Hyperinsulinism:Effect of Exendin-(9-39) on Fasting Adaptation and Protein Sensitivity
The purpose of this study is to examine the effects of exendin-(9-39) on fasting blood
glucose and protein induced hypoglycemia on subjects with Congenital Hyperinsulinism. Funding
Source - FDA Office of Orphan Products Development (OODP).
glucose and protein induced hypoglycemia on subjects with Congenital Hyperinsulinism. Funding
Source - FDA Office of Orphan Products Development (OODP).
This is a placebo controlled study with randomized crossover design to evaluate the effect of
the glucagon-like peptide-1 (GLP-1) receptor antagonist, exendin-(9-39), on fasting blood
glucose levels, protein-induced hypoglycemia, and fasting tolerance of subjects with
congenital hyperinsulinism due to mutations in the ATP- sensitive potassium channel (KATP)
channel.
the glucagon-like peptide-1 (GLP-1) receptor antagonist, exendin-(9-39), on fasting blood
glucose levels, protein-induced hypoglycemia, and fasting tolerance of subjects with
congenital hyperinsulinism due to mutations in the ATP- sensitive potassium channel (KATP)
channel.
Inclusion Criteria:
- Confirmed diagnosis of hyperinsulinism
- Mutation analysis results demonstrating KATP channel defect
- Age 6 months to 18 years with
- Persistent hypoglycemia
Exclusion Criteria:
- Current therapy with medications that may affect glucose metabolism such as
octreotide, diazoxide, high dose glucocorticoids, adrenergic agents, etc. Subjects
will be eligible to participate if the last dose of octreotide is given 48 hrs before
study day 1 and the last dose of diazoxide is given 72 hours before study day 1
- Evidence of a medical condition that might alter results or compromised the
elimination of the peptide, including active infection, kidney failure, severe liver
dysfunction, severe respiratory or cardiac failure
- Pregnancy
- Subjects with milk protein allergy will be excluded for participating in studies
involving protein tolerance test
We found this trial at
1
site
South 34th Street
Philadelphia, Pennsylvania 19104
Philadelphia, Pennsylvania 19104
215-590-1000
Principal Investigator: Diva D De Leon, MD
Phone: 267-426-7622
Children's Hospital of Philadelphia Since its start in 1855 as the nation's first hospital devoted...
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