Recruiting
Phase 2

Pegvisomant

Sponsor:

National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)

Code:

NCT05470504

Conditions

Insulin Receptor Mutation

Partial Lipodystrophy

Eligibility Criteria

Sex: All

Age: 18 - 70

Healthy Volunteers: Not accepted

Interventions

Pegvisomant

Study Details

Brief summary:

Background:

Lipodystrophy (LD) syndromes are a group of rare disorders that affect how a person s body can store and use fat tissue. Many people with LDs become severely insulin resistant. Some people are insulin resistant because of a variant in the insulin receptor gene. Insulin resistance causes many health problems.

Objective:

To learn if blocking the effects of growth hormone in the body will help people with severe insulin resistance.

Eligibility:

Adults aged 18 to 65 years with either a known variant in the insulin receptor gene or with a diagnosis of partial LD.

Design:

Participants will have 2 hospital stays, about 1 month apart. Each stay will be 3 or 4 nights.

During each hospital stay, participants will have many tests. They will have a physical exam with blood tests. They will have all of their urine collected for a 24-hour period. They will have scans to measure their muscle, bone, and fat tissues. They will have tests to measure metabolism and insulin sensitivity. They may have an optional biopsy of fat tissue.

During the first hospital visit, participants will learn how to give themselves shots of a drug (pegvisomant) that blocks growth hormone. The drug is injected under the skin. Participants will continue to give themselves these shots once a day at home.

After the first hospital visit, participants will talk on the phone with members of the study team once each week. After 2 weeks they will have blood drawn for tests.

Participants will stop the shots after the second hospital visit.

Conditions

Insulin Receptor Mutation

Partial Lipodystrophy

Study ID

NCT05470504

Start date

Jan 23, 2023

Status verified date

Aug 14, 2026

Completion date

Jan 30, 2028

Anticipated

Primary completion date

Jan 30, 2028

Anticipated

Eligibility Criteria

Eligibility Criteria

Sex: All

Age: 18 - 70

Healthy Volunteers: Not accepted

  • INCLUSION CRITERIA:

To be eligible to participate in this study, an individual must meet all the following criteria:

  • Either

  • Known pathogenic variant in the insulin receptor gene, either dominant negative or recessive, OR
  • Clinical diagnosis of partial lipodystrophy based on reduction in adipose tissue outside the normal range in selected adipose depots (including, at a minimum, the gluteofemoral depot) with preservation of adipose tissue in other depots.
  • Male or female, aged 18-70 years.
  • Completed linear growth and puberty.

EXCLUSION CRITERIA:

An individual who meets any of the following criteria will be excluded from participation in this study:

  • Use of niacin or other drugs that directly affect lipolysis within 8 weeks prior to enrollment.
  • Patients taking anticoagulants (blood thinning medications).
  • Use of non-steroidal anti-inflammatory medications (e.g., aspirin, ibuprofen) 2 weeks prior to the biopsy date (in patients who choose to undergo biopsy).
  • Changes in medications for diabetes or dyslipidemia within 2 weeks prior to enrollment.
  • Pregnancy or lactation.
  • For females of reproductive potential: inability or unwillingness to use contraception during study participation and for an additional 1 month after the end of pegvisomant administration.
  • For males of reproductive potential: inability or unwillingness to use condoms or other methods to ensure effective contraception with partner during the study and for an additional 1 month after the end of pegvisomant administration.
  • Known allergic reactions pegvisomant or any of its components.
  • Clinically significant liver disease, evidenced by any of the following:

  • ALT or AST >3 times the upper limit of normal at screening.
  • Current known liver disease other than steatohepatitis (e.g., autoimmune or viral hepatitis).
  • History of cirrhosis
  • Triglycerides >1500 mg/dL (non-fasting) or >1000 mg/dL (fasting) at screening.
  • In subjects with partial lipodystrophy only, Hemoglobin A1c >10% at screening.
  • Any other medical condition or medication that, in the judgement of the investigator, will increase risk to the subject or impede the measurement of study outcomes.
  • Inability of subject to understand or the unwillingness to sign a written informed consent document.

Study Design

Enrollment

25 participants

Anticipated

Intervention Model

Single group

Primary purpose

Treatment

Interventions and Outcome Measures

Arms

other: 1

open label pegvisomant

Interventions

Pegvisomant

30 mg subcutaneously every day for 4 weeks.

Primary outcome measure

  • Glycerol rate of appearance (Ra) normalized to fat mass, Palmitate Ra normalized to fat mass [ Time Frame: 1 month ]

Central Contacts and Locations

Central contacts

Megan S Startzell, R.N.

(301) 402-6371megan.startzell@nih.gov

Rebecca J Brown, M.D.

(301) 594-0609brownrebecca@mail.nih.gov

Locations

National Institutes of Health Clinical Center

Recruiting

Bethesda, Maryland, United States, 20892

Contacts

For more information at the NIH Clinical Center contact Office of Patient Recruitment (OPR)

800-411-1222ccopr@nih.gov

More Information

Sponsor

National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)

Last update posted

Aug 18, 2026

Last verified

Aug 14, 2026

Keywords

  • Pegvisomant
  • Severe Insulin Resistance
  • Growth Hormone Inhibition
  • LIPOLYSIS

Trial information was received from ClinicalTrials.gov and was last updated on 2026-09-09. This information was provided to ClinicalTrials.gov by National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK) on 2026-08-18.