Clin2
NCT05470504Possibly a fitRecruiting

Pegvisomant for severe insulin resistance from rare fat or gene problems

Insulin Receptor MutationPartial Lipodystrophy

Part of Hormones & metabolism clinical trials.

This Phase 2 study tests pegvisomant, a medicine that blocks growth hormone, to see if it can improve severe insulin resistance in people with a specific genetic cause or a rare fat distribution condition. If you fit the rare diagnosis, the study may help clarify whether growth-hormone blocking can improve blood sugar and related health markers.

Summary written for real people, not researchers, by Clin2.

Phase
Phase 2
Enrollment
25 people
Ages
18 years to 70 years
Study type
Interventional

Who can take part

  • You have either a known insulin receptor gene change (dominant negative or recessive) OR a diagnosis of partial lipodystrophy with less body fat in certain areas (at least the thigh/hip area).
  • You’re between 18 and 70 years old.
  • You’ve finished linear growth and puberty.
  • You have not used niacin or other medicines that directly affect fat breakdown (lipolysis) within the last 8 weeks.
  • Your diabetes or cholesterol medicines have not changed within the last 2 weeks.
  • You can and will sign the informed consent form and understand what the study involves.

View the official record on ClinicalTrials.gov

Quick eligibility check

Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.

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