Compassionate Use of Metreleptin in Previously Treated People With Partial Lipodystrophy

National Institutes of Health (NIH)

Status and phase

Active, not recruiting

Phase 2

Conditions

Diabetes

Hyperlipidemia

Lipodystrophy

Treatments

Drug: Metreleptin

Study type

Interventional

Funder types

NIH

Identifiers

NCT02262806

150002

15-DK-0002

Details and patient eligibility

About

Background:

Partial lipodystrophy can cause high blood fat levels and resistance to insulin. This can lead to health problems including diabetes. Researchers have found that the drug metreleptin improves health in people with this disease.

Objective:

To test the safety and effectiveness of metreleptin.

Eligibility:

People age 6 months and older with partial lipodystrophy who
have received metreleptin through NIH studies and shown improvement AND
cannot get metreleptin other ways.

Design:

Participants will come to NIH approximately every 6 months during year one, then every 1 2 years. Financial assistance may be available for travel within the U.S.
At visits, participants will get a supply of metreleptin to take home for daily injections, or it can be shipped to them inside the U.S. They will have:
plastic catheter placed in an arm vein.
blood tests, urine collection, and physical exam.
oral glucose tolerance test, drinking a sweet liquid.
ultrasound of the heart, liver, uterus, and ovaries. A gel and a probe are placed on the skin and pictures are taken of the organs.
echocardiogram, which takes pictures of the heart with sound waves.
Resting Metabolic Rate taken. A plastic hood is worn over the head while the oxygen they breathe is measured.
Participants will have up to 3 DEXA scan x-rays per year.
Participants may have:
annual bone x-rays.
liver biopsies every few years. A needle will be inserted into the liver to obtain a small piece. Participants will sign a separate consent for this.
Participants must be seen regularly by their local doctors and have blood tests at least every 3-6 months at home.

Full description

Leptin is an adipocyte-derived hormone that can be thought of as a signal from adipose tissue to the rest of the body conveying information about long-term nutritional status. Patients with lipodystrophy have leptin deficiency secondary to lack of adipose tissue. The combination of leptin deficiency and ectopic lipid deposition in patients with lipodystrophy leads to metabolic complications including severe insulin resistance and diabetes, hypertriglyceridemia, non-alcoholic steatohepatitis, and polycystic ovarian syndrome. Between 2000 and 2014, the NIDDK IRP conducted an open-label clinical trial of the recombinant human leptin analog, metreleptin, in patients with generalized and partial forms of lipodystrophy. This study showed that metreleptin ameliorates metabolic and endocrine abnormalities in lipodystrophy, including reducing food intake, improving insulin resistance and diabetes, reducing ectopic lipid, and normalizing reproduction. Based on these data, metreleptin was approved by the FDA in February, 2014, for patients with generalized, but not partial, lipodystrophy. Our data have shown, however, that a subgroup of patients with partial lipodystrophy do gain medical benefit from metreleptin.

The purpose of this study is twofold:

To provide access to metreleptin to patients with partial lipodystrophy who have previously received and derived benefit from metreleptin through NIH studies (protocols 02-DK-0022 and 13-DK-0057).
To continue to collect data on the long-term efficacy of metreleptin in ameliorating the metabolic complications of partial lipodystrophy.

Metreleptin will be given at doses of less than or equal to 0.24 mg/kg/day, adjusted based on body weight and metabolic control. Patients will be seen approximately once per year at NIH for evaluation, and potentially less frequently for those who are medically stable and have difficulty traveling to NIH. Laboratory evaluation will be obtained more frequently by the patient s home providers as clinically indicated. The primary outcomes of the study are improvements in serum triglycerides and hemoglobin A1c levels. Secondary outcomes include measures of steatohepatitis and ectopic lipid, body composition, bone mineral density and bone mineral metabolism, and pituitary and reproductive function.

Metreleptin is supplied by Chiesi USA, Inc. Neither the NIH nor Chiesi USA, Inc. can guarantee that leptin will be available indefinitely and/or after the study ends.

Enrollment

30 patients

Sex

All

Ages

6 months to 98 years old

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

INCLUSION CRITERIA
Age greater than or equal to 6 months
Partial lipodystrophy (either genetic or acquired)
Previously or currently treated with metreleptin under NIH study 02-DK-0022 and/or NIH study 13-DK-0057.
Documented metabolic benefit from prior or current metreleptin treatment, defined as one or more of the following:
- TG reduction greater than or equal to 30% OR
- HbA1c reduction greater than or equal to 1% OR
- Decrease in insulin requirements greater than or equal to 40% OR
- Decrease in episodes of pancreatitis OR
- Improvement in steatohepatitis OR
- Withdrawal of metreleptin led to marked worsening of metabolic parameters

EXCLUSION CRITERIA

Availability of metreleptin to the patient either as an approved drug, or through local compassionate use or expanded access programs.
Known HIV infection or HIV-associated lipodystrophy.
Psychiatric disorder impeding competence or compliance.
Any medical condition or medication that will increase risk to the subject.
Current alcohol or substance abuse.
Subjects who have a known hypersensitivity to E. coli derived proteins.