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Study identifier: NCT05470504 Synced from ClinicalTrials.gov · July 29, 2026
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Study of Growth Hormone Inhibition Using Pegvisomant in Severe Insulin Resistance

Condition: Insulin Receptor Mutation · Partial Lipodystrophy  ·  Sponsor: National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)

PhasePhase 2
Planned participants25
Who can joinAll sexes, 18 Years to 70 Years
Healthy volunteersNo

About this study

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 …

This description comes directly from the study's public registry record.

Talk to the study team

Megan S Startzell, R.N.  ·  (301) 402-6371  ·  megan.startzell@nih.gov

Rebecca J Brown, M.D.  ·  (301) 594-0609  ·  brownrebecca@mail.nih.gov

Always discuss trial participation with your own doctor first.

Locations (1)

National Institutes of Health Clinical CenterBethesda, Maryland, United StatesRecruiting

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Source record: clinicaltrials.gov/study/NCT05470504