New drug hopes to rebuild muscle in rare disease
NCT ID NCT07435129
First seen Feb 28, 2026 · Last updated Apr 29, 2026 · Updated 5 times
Summary
This study tests a drug called apitegromab in 60 adults with facioscapulohumeral muscular dystrophy (FSHD), a condition that causes muscle weakness. Participants will receive either the drug or a placebo for 52 weeks. The main goal is to see if the drug increases total lean muscle volume, measured by full-body MRI.
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Summaries may miss details or leave out important information. Before applying or accepting participation, make sure you have read and understood the full study. Curemydisease.com takes no responsibility whatsoever for anything missed, misunderstood, or acted upon as a result of our summary — we know it does not capture everything.
This is a summary of the original study . Summaries may miss details or leave out important information. Before applying or accepting participation, make sure you have read and understood the full study. Curemydisease.com takes no responsibility whatsoever for anything missed, misunderstood, or acted upon as a result of our summary — we know it does not capture everything.
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