Capricor Therapeutics shares response to FDA briefing ahead of Deramiocel advisory meeting

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Capricor Therapeutics shares response to FDA briefing ahead of Deramiocel advisory meeting — Capricor responds to FDA briefing

Capricor Therapeutics, Inc. has released its remarks on the recent FDA briefing materials ahead of the anticipated July 29 FDA Advisory Committee meeting for Deramiocel.

The company is taking a proactive approach as regulators prepare to assess its drug candidate for Duchenne muscular dystrophy. Investors and analysts will watch the outcome closely, as the advisory committee’s discussions could shape the future of Deramiocel and Capricor Therapeutics' prospects in the biopharmaceutical sector.

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