Gene therapy trial aims to help boys with duchenne walk stronger

NCT ID NCT07160634

First seen Jun 27, 2026 · Last updated Jun 27, 2026

Summary

This study tests a one-time gene therapy called SGT-003 in 80 boys with Duchenne muscular dystrophy who can still walk. The goal is to see if it helps them move better, like standing up faster and climbing stairs. Participants will receive either the therapy or a placebo first, then switch, and be followed for at least 5 years.

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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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Conditions

The condition(s) this trial relates to.

Duchenne muscular dystrophy

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Contacts and locations

Study contacts

  • Contact

    Phone: •••-•••-•••• Email: •••••@•••••

Locations

  • Arkansas Children's Hospital

    NOT_YET_RECRUITING

    Little Rock, Arkansas, 72202, United States

    Contact Email: •••••@•••••

  • BC Children's Hospital

    RECRUITING

    Vancouver, British Columbia, Canada

    Contact

    Contact Phone: •••-•••-•••• Email: •••••@•••••

  • Children's Hospital of the King's Daughters

    NOT_YET_RECRUITING

    Norfolk, Virginia, 23510, United States

    Contact Email: •••••@•••••

  • Neurology Rare Disease Center

    NOT_YET_RECRUITING

    Flower Mound, Texas, 75082, United States

    Contact Email: •••••@•••••

  • The Children's Hospital of Westmead

    RECRUITING

    Sydney, New South Wales, Australia

    Contact Phone: •••-•••-•••• Email: •••••@•••••

    Contact