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LGMDR9

Clinical trials for LGMDR9 explained in plain language.

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  • Experimental gene therapy targets rare muscle disease

    Disease control Ongoing

    This early-stage trial tests a gene therapy called ATA-100 for people with LGMDR9, a rare genetic muscle disease that causes progressive weakness. Six adults receive a single intravenous infusion of the therapy, which delivers a working copy of the FKRP gene. The main goal is to …

    Matched conditions: LGMDR9

    Phase: PHASE1 • Sponsor: Atamyo Therapeutics • Aim: Disease control

    Last updated Jun 27, 2026 07:54 UTC

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