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Class action filed against Capricor Therapeutics over alleged misleading FDA approval info

Market News
03 Aug 2026
Bronstein, Gewirtz & Grossman Llc
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Bearish
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A class action lawsuit has been filed against Capricor Therapeutics and some of its officers for allegedly making false statements about FDA approval risks related to their drug Deramiocel. The complaint claims Capricor changed its clinical data analysis without FDA agreement, risking the drug's approval for Duchenne muscular dystrophy. Investors who bought Capricor securities between December 17, 2025, and July 26, 2026, are encouraged to join the lawsuit by September 28, 2026. The law firm Bronstein, Gewirtz & Grossman is representing affected investors on a contingency fee basis, aiming to recover damages for those harmed by the alleged securities violations.

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