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Capricor Therapeutics shares plummeted 67.7% following market warning signs and a negative vote from a U.S. FDA expert panel. The panel rejected effectiveness data for the company's cell therapy targeting Duchenne muscular dystrophy-related heart conditions. Consequently, law firms initiated investigations into potential federal securities law violations following reports of a failed Phase 3 trial. These developments led to a further 60% drop in premarket trading on July 30.