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New hope for FSHD: antibody drug aims to slow muscle loss

NCT ID NCT05548556

First seen Nov 01, 2025 · Last updated May 01, 2026 · Updated 19 times

Summary

This study tests an experimental antibody called RO7204239 in 51 adults with facioscapulohumeral muscular dystrophy (FSHD), a genetic disease that causes progressive muscle weakness. The drug blocks a protein that limits muscle growth, with the goal of preserving or increasing muscle volume. Participants receive either the drug or a placebo, and researchers measure changes in muscle size and safety over time.

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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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Contacts and locations

Locations

  • Asst Grande Ospedale Metropolitano Niguarda

    Milan, Lombardy, 20162, Italy

  • Kennedy Krieger Institute

    Baltimore, Maryland, 21205, United States

  • National Hospital for Neurology and Neurosurgery,

    London, WC1N 3BG, United Kingdom

  • Policlinico Universitario Agostino Gemelli

    Rome, Lazio, 00168, Italy

  • Regents of the University of Colorado

    Aurora, Colorado, 80045, United States

  • Rigshospitalet

    København Ø, 2100, Denmark

  • Royal Victoria Infirmary

    Newcastle upon Tyne, NE1 4LP, United Kingdom

  • University of Irvine Medical Center (UCIMC)

    Orange, California, 92868, United States

  • University of Kansas Medical Center

    Fairway, Kansas, 66205, United States

  • Virginia Commonwealth University Medical Center

    Richmond, Virginia, 23298-0599, United States

Conditions

Explore the condition pages connected to this study.