Capricor Therapeutics completes submission of biologics license application to the US FDA for deramiocel for the treatment of Duchenne muscular dystrophy

Capricor Therapeutics

2 January 2024 - If approved, deramiocel would be first approved therapy for Duchenne muscular dystrophy cardiomyopathy.

Capricor Therapeutics today announced the completion of the submission of its biologics license application to the US FDA seeking full approval for deramiocel, an investigational cell therapy, to treat patients diagnosed with Duchenne muscular dystrophy cardiomyopathy.

Read Capricor Therapeutics press release

Michael Wonder

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Michael Wonder

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US , Dossier , Cellular therapy