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JAR914 is an investigational therapeutic being developed by JAR of Hope for **Duchenne muscular dystrophy**, a rare, progressive, and fatal muscle-wasting disorder. Based on the provided source context, JAR914 had an FDA-cleared IND in March 2021 to begin a small clinical study in up to 12 children focused on safety and efficacy. The exact molecular composition, modality, route, and target have not been clearly disclosed in the provided materials, so its precise mechanism of action cannot be stated with confidence from the available evidence.
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