FSHD2
Clinical trials for FSHD2 explained in plain language.
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New hope for FSHD: phase 3 trial of AOC 1020 begins
Disease control Recruiting nowThis study tests an experimental drug called AOC 1020 for facioscapulohumeral muscular dystrophy (FSHD), a genetic condition that causes progressive muscle weakness. About 200 adults with a confirmed FSHD diagnosis who can still walk will receive either the drug or a placebo by I…
Matched conditions: FSHD2
Phase: PHASE3 • Sponsor: Avidity Biosciences, Inc. • Aim: Disease control
Last updated May 26, 2026 08:32 UTC
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New study uses sound waves to monitor breathing in rare muscle disease
Knowledge-focused Recruiting nowThis study follows 34 adults with FSHD for one year to see how their breathing muscles change over time. Researchers will use ultrasound and breathing tests to measure diaphragm function. The goal is to find better ways to detect and track breathing problems in FSHD.
Matched conditions: FSHD2
Phase: NA • Sponsor: Fondazione Policlinico Universitario Agostino Gemelli IRCCS • Aim: Knowledge-focused
Last updated May 26, 2026 08:37 UTC
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New registry aims to unlock FSHD mysteries through patient data
Knowledge-focused Recruiting nowThis study creates a registry for people with facioscapulohumeral muscular dystrophy (FSHD) to share their health experiences and data. Up to 5,000 participants in the U.S. will provide information on symptoms, progression, and quality of life. The goal is to help researchers bet…
Matched conditions: FSHD2
Sponsor: FSHD Society • Aim: Knowledge-focused
Last updated May 19, 2026 11:47 UTC