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
3
Locations
1
Results
Posted
Publications
12
Study summary
This study will test the hypothesis that leptin contributes to the regulation of the dynamics of human endocrine function.
The study aims to elucidate the role of leptin in the regulation of human endocrine function approached by a carefully designed, prospective clinical study of the rapidly-sampled dynamics of endocrine rhythms during the course of leptin-replacement treatment in the only three adult individuals identified in the world so far who are leptin-naive due to a functional leptin gene mutation. A study of leptin-naive subjects avoids all confounding factors and pitfalls, because the only bioactive leptin to which they will be exposed is the exogenously administered recombinant protein. Thus, this proposal will permit us to ascertain the endocrine effects of human leptin.
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 14, 2008
Study start
Jun 2001
Primary completion
May 4, 2010
Study completion
May 4, 2010
Results posted
Feb 13, 2020
Registry updated
Feb 13, 2020
Outcomes
Change in Weight
Time frame · Baseline, 107 months
Change in Glucose Levels
Time frame · Baseline, 107 months
Eligibility
Inclusion Criteria: * Congenital leptin deficiency (these are only 3 adult individuals in the world that have been identified as leptin-naïve thus far). Exclusion Criteria: * Pregnant, trying to become pregnant, breast-feeding an infant or sexually active women, not using contraception. * Subjects with hemoglobin levels below 12 g/dl. * Subjects whose body contains a ferromagnetic implanted device that might produce a safety hazard during fMRI.
Study locations
United States. Showing up to 24 locations stored in the fast local snapshot.
University of Miami Miller School of Medicine, Center on Pharmacogenomics
Miami, Florida, United States
Publications
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