Clin2
NCT07798609Possibly a fitRecruiting

Testing SFL-0821 for people with FSHD

Facioscapulohumeral Muscular Dystrophy (FSHD)

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

This study is testing a new medicine, SFL-0821, to see if it is safe and useful for people with FSHD. It may help if it works, but it is still experimental.

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

Phase
Phase 1/Phase 2
Enrollment
90 people
Ages
18 years to 65 years
Study type
Interventional

Who can take part

  • Confirmed FSHD type 1 or 2 by genetic testing
  • Disease severity within a specific range (Clinical Severity Score 1.5 to 4)
  • Can walk 10 meters in 5 to 14 seconds, using at most a cane or ankle brace
  • Willing to have a muscle biopsy before and after the study drug

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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