Trial of Leptin Replacement Therapy in Patients With Lipodystrophy



Status:Completed
Conditions:Endocrine
Therapuetic Areas:Endocrinology
Healthy:No
Age Range:6 - 70
Updated:4/4/2019
Start Date:April 2006
End Date:November 2014

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Double-Blind, Placebo-Controlled Trial of Leptin Replacement Therapy in Patients With Lipodystrophy

Lipodystrophies represent a therapeutic challenge with regards to insulin resistance,
hypertriglyceridemia and fatty liver which often is coupled with significant adipose tissue
loss. The purpose of the study is to examine the safety and efficacy of Leptin on subjects
with lipodystrophy.

The mechanism by which leptin improves glucose and lipid control is not clear. We will
examine the possible mechanisms of leptin action by studying the effects of leptin
administration on food intake, insulin resistance, insulin secretory response, hepatic and
intramuscular triglyceride stores in a large sample of patients with lipodystrophy.

Hypothesis: Leptin replacement in patients with generalized and partial lipodystrophy and
hypoleptinemia will be safe and efficacious in improving the metabolic abnormalities
associated with insulin resistance.

Inclusion Criteria:

- age > 6 years

- Partial and generalized lipodystrophy

- Serum leptin levels less than the 7th percentile of normal values reported by the 3rd
National Health and Nutrition Examination survey (less than 7.0 ng/mL in females and
less than 3/0 ng/mL in males)

- Presence of at least one of the following metabolic abnormalities:

1. Type 2 Diabetes Mellitus

2. Fasting serum insulin >20 uU/mL

3. Fasting serum triglycerides > 300 mg/dL

4. Previous participation in leptin trial (Amgen 991265, GCRC 660) - for Part B of
the Study.

Exclusion Criteria:

- Known liver disease due to causes other than non-alcoholic steatohepatitis.

- Hematocrit of less than 30%.

- Current alcohol or substance abuse.

- Use of anorexigenic drugs, anabolic steroids, GH and thiazolidinediones

- Active tuberculosis

- Psychiatric disorder impeding competence or compliance

- Malignancies

- HIV infection

- Subjects who have a known hypersensitivity to E. Coli derived proteins

- Other condition, which in the opinion of the clinical investigators would impede
completion of the study.
We found this trial at
1
site
2201 Inwood Rd
Dallas, Texas 75235
(214) 645-8300
U.T. Southwestern Medical Center The story of UT Southwestern Medical Center is one of commitment...
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