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The Cellular, Tissue and Gene Therapies Advisory Committee voted 3-9 that available evidence does not support Deramiocel's effectiveness for DMD cardiomyopathy. The vote is non-binding and addressed a narrower indication than proposed; the PDUFA target action date remains August 22, 2026.
EX-99 2 capr-20260729xex99.htm EX-99 Exhibit 99.1 Capricor Therapeutics Provides Update on FDA Advisory Committee Meeting for Deramiocel SAN DIEGO , July 30, 2026 (GLOBE NEWSWIRE) — Capricor Therapeutics (NASDAQ: CAPR), a biotechnology company developing transformative cell and exosome-based therapeutics for rare diseases, today announced that the U.S. Food and Drug Administration's Cellular, Tissue and Gene Therapies Advisory Committee voted that available evidence did not support the effectiveness of Deramiocel for the treatment of cardiomyopathy in patients with Duchenne muscular dystrophy (DMD), a rare and life-threatening disease for which there is no approved treatment for this cardiac complication (3 for, 9 against, 0 abstain). The Committee's vote is non-binding. The Committee's v
Capricor sẽ trình bày dữ liệu HOPE-2 OLE 5 năm và HOPE-3 Ph3 tại PPMD 2026