Record mula sa primary source
Tinanggap ng FDA ang Class 2 resubmission at ipinagpatuloy ang buong pagsusuri ng Deramiocel BLA para sa DMD, na nagtakda ng PDUFA target action date na Agosto 22, 2026. Inaasahang magsisimula na ang mga talakayan tungkol sa labeling. Natugunan ng HOPE-3 Phase 3 trial ang pangunahing endpoint nito at lahat ng Type I error-controlled secondary endpoints, na sumusuporta sa BLA.
EX-99.1 2 capr-20260512xex99d1.htm EX-99.1 Exhibit 99.1 Capricor Therapeutics Reports First Quarter 2026 Financial Results and Provides Corporate Update ● Deramiocel BLA under active FDA review; PDUFA target action date of August 22, 2026; labeling discussions expected to commence soon ● HOPE-3 Phase 3 trial met its primary endpoint (PUL v2.0; upper limb function) and all Type I error-controlled secondary endpoints ● GMP manufacturing facility fully operational; second-floor expansion well underway ● Chief Commercial Officer with direct DMD commercial experience expected to join the Company in the coming weeks ● Filed suit against Nippon Shinyaku Co., Ltd. and NS Pharma, Inc. seeking rescission of U.S. distribution agreement and preliminary injunction; FDA review and PDUFA date unaffecte
Capricor ipapakita ang 5-taong HOPE-2 OLE at HOPE-3 Ph3 data sa PPMD 2026