DRUG
Recombinant methionyl human leptin
Recombinant methionyl human leptin, subcutaneous, once a day, 0.02 to 0.04 mg/kg (adjusted according to weight loss), indeterminate duration.
Status
Completed
Phase
Phase 2
Enrollment
1
Locations
1
Results
Posted
Publications
12
Study summary
To assess the endocrine and immune effects of leptin replacement in leptin-deficient children, from a consanguineous family. The hypothesis is that leptin replacement will have significant effects on endocrine function.
The proposed study of the treatment of a child with congenital leptin deficiency will permit to elucidate key aspects of human endocrine function, and will give new insights on the role of leptin in human endocrine regulation.
Interventions
DRUG
Recombinant methionyl human leptin, subcutaneous, once a day, 0.02 to 0.04 mg/kg (adjusted according to weight loss), indeterminate duration.
Timeline
First posted
Apr 16, 2008
Study start
Jun 2005
Primary completion
Apr 16, 2010
Study completion
Apr 16, 2010
Results posted
Feb 13, 2020
Registry updated
Feb 13, 2020
Outcomes
Weight
Time frame · Baseline, 58 months
Glucose Levels
Time frame · Baseline, 58 months
Bone Mineral Density
Time frame · Baseline, 58 months
Eligibility
Inclusion Criteria: * Children with a functional leptin gene mutation from a consanguineous Turkish family. Only one leptin-naïve child from this family is alive and eligible. Exclusion Criteria: * N/A
Study locations
United States. Showing up to 24 locations stored in the fast local snapshot.
University of Miami, Center on Pharmacogenomics
Miami, Florida, United States
Publications
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