An Investigator-initiated Clinical Study Evaluating the CRISPR-hfCas12Max Gene Editing Therapy in the Treatment of Duchenne Muscular Dystrophy (DMD)
Latest Information Update: 06 Aug 2026
At a glance
- Drugs HG 302 (Primary)
- Indications Duchenne muscular dystrophy
- Focus Adverse reactions
- Acronyms MUSCLE
- Sponsors HuidaGene Therapeutics
Most Recent Events
- 03 Aug 2026 Planned End Date changed from 30 Sep 2026 to 2 Jun 2027.
- 03 Aug 2026 Planned primary completion date changed from 30 Sep 2026 to 2 Aug 2026.
- 03 Aug 2026 Status changed from completed to active, no longer recruiting.