Record mula sa primary source
Inuri ng FDA ang susog sa BLA noong Hulyo 2026 bilang pangunahing susog at pinalawig ang target na petsa ng aksyon ng PDUFA mula Agosto 22, 2026 hanggang Nobyembre 22, 2026. Kasama sa susog ang 24-buwang datos mula sa open-label extension ng HOPE-3 at karagdagang pagsusuri na sumusuporta sa pino na indikasyon na nakatuon sa upper limb function. Nagbibigay ang extension sa CBER ng tatlong karagdagang buwan upang suriin ang bagong datos.
EX-99.1 2 capr-20260824xex99d1.htm EX-99.1 Exhibit 99.1 Capricor Therapeutics Announces Extension of PDUFA Target Action Date as FDA Continues Review of Deramiocel BLA – New PDUFA target action date of November 22, 2026 follows submission of additional Phase 3 HOPE-3 data and analyses supporting a refined proposed indication – SAN DIEGO , Aug. 24, 2026 (GLOBE NEWSWIRE) — Capricor Therapeutics (NASDAQ: CAPR), a biotechnology company developing transformative cell and exosome-based therapeutics for the treatment of rare diseases, today announced that the U.S. Food and Drug Administration (FDA) has extended the Prescription Drug User Fee Act (PDUFA) target action date for its Biologics License Application (BLA) for Deramiocel, an investigational cell therapy for Duchenne muscular dystrophy (
Capricor ipapakita ang 5-taong HOPE-2 OLE at HOPE-3 Ph3 data sa PPMD 2026