New study tracks rare muscle disease to uncover its secrets

NCT ID NCT05046821

First seen Feb 19, 2026 · Last updated Apr 30, 2026 · Updated 14 times

Summary

This study follows 150 adults with sporadic inclusion body myositis, a rare muscle-weakening disease, for two years. Researchers will measure muscle strength, swallowing, breathing, and blood markers every six months. The goal is to learn how the disease progresses, not to test a new treatment.

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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

  • Brigham and Women's Hospital

    Boston, Massachusetts, 02115, United States

  • Johns Hopkins University

    Baltimore, Maryland, 21287, United States

  • Kansas University Medical Center

    Fairway, Kansas, 66205, United States

  • Nerve and Muscle Center of Texas

    Houston, Texas, 77030, United States

  • Ohio State University

    Columbus, Ohio, 43221, United States

  • Oregon Health & Science University

    Portland, Oregon, 97239, United States

  • University of California, Irvine

    Orange, California, 92868, United States

  • University of California, Los Angeles

    Los Angeles, California, 90095, United States

  • University of Colorado

    Aurora, Colorado, 80045, United States

  • University of Miami

    Miami, Florida, 33136, United States

  • University of Pennsylvania

    Philadelphia, Pennsylvania, 19104, United States

  • University of Washington

    Seattle, Washington, 98195, United States

  • Washington University in St. Louis

    St Louis, Missouri, 63110, United States

Conditions

Explore the condition pages connected to this study.