Expanded Access Metreleptin Study

NCT ID: NCT02404896

Last Updated: 2025-02-17

Basic Information

• Recruitment Status: AVAILABLE
• Study Classification: EXPANDED_ACCESS

Brief Summary

Metreleptin was approved in the United States as adjunct to diet as replacement therapy to treat the complications of leptin deficiency in patients with congenital or acquired generalized lipodystrophy in February 2014. The approval was based on results obtained in 2 open-label, investigator-sponsored studies (Studies 991265 and 20010769) conducted at the National Institutes of Health (NIH) to evaluate the safety and efficacy of metreleptin treatment in patients with lipodystrophy and 1 treatment IND (FHA101/MB002-002/MB002-002) conducted by Bristol-Myers Squibb on behalf of AstraZeneca (BMS/AZ) in patients with diabetes mellitus and/or hypertriglyceridemia related to lipodystrophy. These studies enrolled patients with lipodystrophy including both generalized and partial lipodystrophy. Although the marketing authorization restricted the indication to patients with generalized lipodystrophy, meaningful clinical benefit was achieved in a subset of patients with partial lipodystrophy, and these patients from FHA101/MB002-002 form the basis of the request for ongoing treatment under expanded access.

Detailed Description

Leptin is a naturally occurring hormone and an important regulator of energy homeostasis and other diverse physiological functions. Circulating levels of leptin closely correlate with the amount of adipose tissue present. Metreleptin, a recombinant analogue of human leptin, is a 147-amino acid polypeptide that differs from the human leptin sequence by 1 additional amino acid, methionine, located at the amino-terminal end. Metreleptin has the same physiological effects as leptin, including regulation of energy homeostasis and metabolic function.

The patient group covered under this expanded access submission has demonstrated evidence of clinical benefit from treatment with metreleptin in clinical study FHA101/MB002-002, and needs expanded access to continue treatment without interruption.

New enrollment, subject to approval by the FDA, can be considered on a case-by-case basis.

Conditions

Familial Partial Lipodystrophy

Interventions

Metreleptin

Metreleptin open-label treatment

Intervention Type: DRUG

Other Intervention Names

MyaLept

Eligibility Criteria

Inclusion Criteria

1. Signed Written Informed Consent

a) Before any program procedures are performed, the details of the program will be described to the patient and the patient will be given a written informed consent document to read. If the patient agrees to participate in the program, consent will be indicated by signing and dating of the informed consent document in the presence of program personnel.

2. Target Population

1. Ability to comply with visits and procedures required by program

2. Previously enrolled in study FHA101/MB002-002

3. Has physician-confirmed partial lipodystrophy and had evidence of benefit with metreleptin treatment based on the following metabolic criteria demonstrated within the last year of metreleptin treatment (if on treatment over 1 year) from baseline values:

• TG reduction ≥ 30% OR
• HbA1c reduction ≥ 1% OR
• Decrease in insulin requirements ≥ 40% OR
• Decrease in episodes of pancreatitis OR
• Improvement in steatohepatitis OR
• Withdrawal of metreleptin led to marked worsening of metabolic parameters

3. Age and Reproductive Status

1. Male or female, over the age of 6 months

2. Women of childbearing potential (WOCBP) must have a negative serum or urine pregnancy test (minimum sensitivity 25 IU/L or equivalent units of HCG) within 24 hours prior to the restart of study drug.

3. Women must not be breastfeeding

4. WOCBP must agree to follow instructions for method(s) of contraception for the duration of treatment with metreleptin plus 5 half-lives of metreleptin plus 30 days (duration of ovulatory cycle) for a total of 6 months post-treatment completion.

5. Men who are sexually active with WOCBP must agree to follow instructions for method(s) of contraception for the duration of treatment with metreleptin plus 5 half-lives of the metreleptin plus 90 days (duration of sperm turnover) for a total of 3 months post-treatment completion.

Exclusion Criteria

1. Target Disease Exceptions

a) Has acquired lipodystrophy and clinically significant hematologic abnormalities (such as neutropenia and/or lymphadenopathy)

2. Medical History and Concurrent Diseases

1. Has been diagnosed with generalized lipodystrophy

2. Has been diagnosed with HIV infection

3. Has a clinically significant medical condition that could potentially affect the risk/benefit ratio for metreleptin treatment and/or the personal well-being of the patient, as judged by the primary treating physician

4. Has known infectious liver disease

5. Has known allergies to E. coli-derived proteins or hypersensitivity to any component of metreleptin treatment

1. Prisoners or patients who are involuntarily incarcerated.

2. Patients who are compulsorily detained for treatment of either a psychiatric or physical (eg, infectious disease) illness.

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

University of Michigan

OTHER

Sponsor Role: lead

Responsible Party

Elif Oral

Professor, Internal Medicine

Responsibility Role: PRINCIPAL_INVESTIGATOR

Principal Investigators

Elif A Oral, MD

Role: PRINCIPAL_INVESTIGATOR

University of Michigan

Locations

University of Michigan

Ann Arbor, Michigan, United States

Site Status: AVAILABLE

Countries

United States

Central Contacts

Elif A Oral, MD

Role: CONTACT

eliforal@med.umich.edu

734-615-7271

Adam H Neidert, MS

Role: CONTACT

aneidert@med.umich.edu

734-615-0539

Facility Contacts

Elif A Oral, MD

Role: primary

eliforal@med.umich.edu

734-615-7271

Adam H Neidert, MS

Role: backup

aneidert@med.umich.edu

734-615-0539

Other Identifiers

HUM00094843

Identifier Type: -

Identifier Source: org_study_id