Clin2
NCT07642635Possibly a fitNot yet recruiting

GLP-1 drugs to reduce metabolic risk in Duchenne muscular dystrophy

Duchenne Muscular Dystrophy (DMD)

Treatments studied

Part of Bones, joints & muscles, Brain & nervous system, Genetic & congenital, Hormones & metabolism clinical trials.

This trial tests whether a diabetes medication called a GLP-1 receptor agonist (semaglutide) can help people with Duchenne muscular dystrophy manage weight and reduce metabolic complications like high blood pressure and high cholesterol. The medication may help protect heart and metabolic health in this population.

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

Phase
Phase 1/Phase 2
Enrollment
30 people
Ages
18 years and older
Study type
Interventional

Who can take part

  • You are male and at least 18 years old
  • You have a BMI (body mass index) of 30 or higher, OR a BMI of 27+ with a weight-related condition like high blood pressure, type 2 diabetes, or high cholesterol
  • You have been diagnosed with Duchenne muscular dystrophy (confirmed by muscle biopsy or genetic test)
  • You do not have type 1 diabetes, uncontrolled type 2 diabetes, or take insulin or certain diabetes pills
  • You have no history of pancreatitis (pancreas inflammation) or thyroid cancer in your family
  • You are able to undergo MRI scans and tolerate study procedures safely

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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