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Cure Rare Disease gets FDA approval to administer first-in-human CRISPR therapeutic

The U.S. Food and Drug Administration has granted approval for Cure Rare Disease to administer its first-in-human CRISPR therapeutic, according to a press release. The therapeutic, CRD-TMH-001, aims to stop the progression of Duchenne muscular dystrophy in single-patient dosing. The first patient is expected to be dosed at UMass Chan...

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