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An Investigator-initiated Clinical Study Evaluating the CRISPR-hfCas12Max Gene Editing Therapy in the Treatment of Duchenne Muscular Dystrophy (DMD)

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Trial Profile

An Investigator-initiated Clinical Study Evaluating the CRISPR-hfCas12Max Gene Editing Therapy in the Treatment of Duchenne Muscular Dystrophy (DMD)

Status: Recruiting
Phase of Trial: Phase II

Latest Information Update: 28 Nov 2024

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At a glance

  • Drugs HG 302 (Primary)
  • Indications Duchenne muscular dystrophy
  • Focus Adverse reactions
  • Acronyms MUSCLE
  • Sponsors HuidaGene Therapeutics

    • Most Recent Events

    • 25 Nov 2024 Status changed from not yet recruiting to recruiting.
    • 30 Sep 2024 The protocol has been amended to Interventional Study Model as Sequential Assignment.
    • 23 Sep 2024 New trial record

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