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Capricor Therapeutics Faces Shareholder Lawsuit Over Deramiocel Disclosures

Investors who incurred losses in Capricor Therapeutics, Inc. between December 17, 2025, and July 26, 2026, have until September 28 to seek lead plaintiff status in a securities fraud class action. The litigation centers on allegations that the company misled stakeholders regarding the regulatory path for its drug, Deramiocel.

Capricor Therapeutics Faces Shareholder Lawsuit Over Deramiocel Disclosures

The lawsuit, filed by Glancy Prongay Wolke & Rotter LLP, alleges that Capricor Therapeutics failed to disclose critical modifications to the statistical analysis plan used for Deramiocel clinical data. According to the complaint, the company neglected to inform investors that the FDA had not authorized these changes prior to the BLA resubmission. Plaintiffs contend this omission created a significant risk that the drug would fail to demonstrate substantial evidence of effectiveness, jeopardizing regulatory approval for the treatment of Duchenne muscular dystrophy.

Shareholders who purchased securities during the specified period may act as lead plaintiffs or remain absent class members while the case proceeds. Glancy Prongay Wolke & Rotter LLP, a firm recognized for its work in investor recovery, is managing the outreach. Interested parties are directed to contact the firm by September 28, 2026, to participate in the ongoing litigation.

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