Clin2
NCT06643442Possibly a fitNot yet recruiting

Repurposing empagliflozin for children with Duchenne muscular dystrophy and heart problems

DMD-associated Dilated Cardiomyopathy

Treatments studied

Part of Genetic & congenital, Heart & circulation clinical trials.

This trial studies whether a medicine called empagliflozin, currently used for diabetes, can help improve heart function in children with Duchenne muscular dystrophy who also have heart muscle weakness. The medicine is given as a pill and aims to slow down the heart damage so children can feel better for longer.

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

Phase
Phase 2
Enrollment
12 people
Ages
6 years to 18 years
Study type
Interventional

Who can take part

  • Child or teen between 6 and 18 years old
  • Diagnosed with Duchenne muscular dystrophy and related heart problems (cardiomyopathy)
  • Currently taking medication for heart failure
  • Able to have a cardiac MRI without general anesthesia
  • No diabetes or conditions that cause low blood sugar
  • Weight at least 15 kg (about 33 pounds)
  • No recent major surgery, blood transfusion, or upcoming heart surgery
  • Not taking part in another clinical trial right now

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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