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The Gross Law Firm Reminds Capricor Investors of the Pending Class Action Lawsuit with a Lead Plaintiff Deadline of September 15, 2025 - CAPR

NEW YORK, Sept. 04, 2025 (GLOBE NEWSWIRE) -- The Gross Law Firm issues the following notice to sh...

articleCaprock Mining CorpSeptember 4, 20254/company/caprock-mining-corp/news/the-gross-law-firm-reminds-capricor-investors-of-the-pending-class-action-lawsuit-with-a-lead-plaintiff-deadline-of-september-15-2025-capr
The Gross Law Firm Reminds Capricor Investors of the Pending Class Action Lawsuit with a Lead Plaintiff Deadline of September 15, 2025 - CAPR

About this update from Caprock Mining Corp

[{"type":"text","content":"The Gross Law Firm Reminds Capricor Investors of the Pending Class Action Lawsuit with a Lead Plaintiff Deadline of September 15, 2025 – CAPR\n\n\n\n NEW YORK, Sept. 04, 2025 (GLOBE NEWSWIRE) -- The Gross Law Firm issues the following notice to shareholders of\n \n Capricor Therapeutics, Inc. (NASDAQ: CAPR).\n \n\n\n Shareholders who purchased shares of CAPR during the class period listed are encouraged to contact the firm regarding possible lead plaintiff appointment. Appointment as lead plaintiff is not required to partake in any recovery.\n \n\n CONTACT US HERE:\n \n\n\n https://securitiesclasslaw.com/securities/capricor-loss-submission-form/?id=165018&from=3\n \n\n\n\n CLASS PERIOD:\n \n October 9, 2024 to July 10, 2025\n \n\n\n ALLEGATIONS:\n \n According to the complaint, defendants provided investors with material information concerning Capricor’s lead cell therapy candidate drug deramiocel for the treatment of cardiomyopathy associated with Duchenne muscular dystrophy (DMD). Defendants’ statements included, among other things, Capricor’s ability to obtain a Biologics License Application (BLA) for deramiocel from the U.S. Food and Drug Administration (FDA). Defendants provided these overwhelmingly positive statements to investors while, at the same time, disseminating false and misleading statements and/or concealing material adverse facts concerning its four-year safety and efficacy data from its Phase 2 HOPE-2 trial study of deramiocel. On July 11, 2025, Capricor issued a press release announcing it received a Complete Response Letter (CRL) from the FDA denying the BLA specifically citing it did not meet the statutory requirement for substantial evidence of effectiveness and the need for additional clinical data. Further, the CRL referenced outstanding items in the Chemistry, Manufacturing, and Controls section of the application. Following this news, the price of Capricor stock declined from $11.40 per share on July 10, 2025 to $7.64 per share on July 11, 2025.\n \n\n\n DEADLINE: September 15, 2025\n \n Shareholders should not delay in registering for this class action. Register your information here: https://securitiesclasslaw.com/securities/capricor-loss-submission-form/?id=165018&from=3\n \n\n\n NEXT STEPS FOR SHAREHOLDERS:\n \n Once you register as a shareholder who purchased sha...

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