drugset / Trial / NCT00085982

Effect of Metreleptin Therapy in the Treatment of Severe Insulin Resistance

NCT00085982

NaSingle-groupOpen-labelTreatment

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).

Timeline

Start
2003-08-21
Primary completion
2019-10-23
Completion
2030-01-01

Drugs

EvaluationDrugModalityDoseRoute
Subject Metreleptin Protein / enzyme biologic 0.2 mg/kg Subcutaneous
Subject Metreleptin Protein / enzyme biologic 300 mg Subcutaneous