Gene therapy safety tracked for a decade in duchenne patients

NCT ID NCT05689164

First seen Nov 01, 2025 · Last updated May 12, 2026 · Updated 24 times

Summary

This study checks the long-term safety and effects of an experimental gene therapy called fordadistrogene movaparvovec in people with Duchenne muscular dystrophy who already received it in an earlier study. Participants will be followed for 10 years with yearly visits. The goal is to monitor side effects and see how well the therapy works over time.

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Contacts and locations

Locations

  • Duke Children's Health Center

    Durham, North Carolina, 27710, United States

  • Duke Lenox Baker Children's

    Durham, North Carolina, 27705, United States

  • Primary Children's Hospital

    Salt Lake City, Utah, 84113, United States

  • Reed Neurological Research Center

    Los Angeles, California, 90095, United States

  • UCLA Children's Heart Center

    Los Angeles, California, 90095, United States

  • UCLA Clinical Lab Services

    Los Angeles, California, 90095, United States

  • UCLA Kameron Gait and Motion Analysis Laboratory (Westwood Rehabilitation Center)

    Los Angeles, California, 90095, United States

  • UCLA Medical Center

    Los Angeles, California, 90095, United States

  • University of Utah Clinical Neurosciences Center

    Salt Lake City, Utah, 84132, United States

  • University of Utah Craig H. Neilsen Rehabilitation Hospital

    Salt Lake City, Utah, 84132, United States

  • University of Utah Hospital

    Salt Lake City, Utah, 84112, United States

  • University of Utah Imaging and Neurosciences Center

    Salt Lake City, Utah, 84108, United States

Conditions

Explore the condition pages connected to this study.