Clin2
NCT06721299Possibly a fitRecruiting

Testing clenbuterol for muscle health in FSHD

Muscular Dystrophy, Facioscapulohumeral

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

This study tests a medication called clenbuterol to see if it can reduce activity of the DUX4 gene, which is believed to cause muscle damage in FSHD. If you have FSHD type 1 or 2, you may be able to join and help researchers understand if this drug can improve muscle health.

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

Phase
Phase 1
Enrollment
30 people
Ages
18 years to 75 years
Study type
Interventional

Who can take part

  • You have a genetic test confirming FSHD type 1 or 2, or a first-degree relative with a confirmed mutation
  • You are between 18 and 75 years old
  • You can walk 30 feet without help from another person
  • You are able to move your ankle upward against gravity (anti-gravity motion) in at least one leg, or have a leg muscle that appears suitable for a needle biopsy on an MRI
  • You are not currently taking certain medications like beta-blockers, steroids, blood thinners, or GLP-1 drugs (Ozempic-like), and you are not pregnant or planning pregnancy during the study

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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