Myonexus Therapeutics receives FDA orphan drug designation for LGMD type 2E treatment

Myonexus Therapeutics, a clinical-stage gene therapy company developing first ever corrective gene therapies for limb girdle muscular dystrophies, and Nationwide Children’s Hospital announce the U.S. Food and Drug Administration (FDA) has granted Orphan Drug designation to Myonexus’ lead candidate, MYO-101, for the treatment of limb girdle muscular dystrophy (LGMD) type 2E.

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