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Effect of Metreleptin Therapy in the Treatment of Severe Insulin Resistance
Sponsor: National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Summary
Study Description: Patients with mutations of the insulin receptor have diabetes that is challenging to control with conventional therapies, leading to early morbidity and mortality. We hypothesize that recombinant leptin (metreleptin) in these patients will improve glycemia control. Objectives: Primary Objective: To determine if 1 year of metreleptin will improve glycemia control in patients with genetic defects of the insulin receptor. Secondary Objectives: To determine mechanisms by which metreleptin improves glycemia. Endpoints: Primary Endpoint: Hemoglobin A1c. Secondary Endpoints: fasting plasma glucose, fasting insulin/C-peptide, glucose/insulin/C-peptide area under the curve during oral glucose tolerance test. Study Population: 20 male or female patients with mutations of the insulin receptor, age (Bullet)5 years, at the NIH Clinical Center. Description of Sites/Facilities Enrolling Participants: Description of Study Intervention: NIH Clinical Center Open label study of metreleptin, 0.2 mg/kg/day (max dose 0.24 mg/kg/day).
Official title: Phase II Trial of Effect of Metreleptin Therapy in Severe Insulin Resistance
Key Details
Gender
All
Age Range
5 Years - Any
Study Type
INTERVENTIONAL
Enrollment
11
Start Date
2003-08-21
Completion Date
2030-01-01
Last Updated
2025-01-30
Healthy Volunteers
No
Conditions
Interventions
Metreleptin
Administered SC twice/day to achieve physiological concentrations that will be effective in improving the severe state of insulin resistance seen in patients with genetic defects on their insulin receptor mutation
Locations (1)
National Institutes of Health Clinical Center, 9000 Rockville Pike
Bethesda, Maryland, United States