บันทึกจากแหล่งปฐมภูมิ
The FDA has accepted the Class 2 resubmission and resumed full review of the Deramiocel BLA for DMD, setting a PDUFA target action date of August 22, 2026. Labeling discussions are expected to begin soon. The HOPE-3 Phase 3 trial met its primary endpoint and all Type I error-controlled secondary endpoints, supporting the 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 จะนำเสนอข้อมูล HOPE-2 OLE ระยะ 5 ปี และข้อมูล HOPE-3 Ph3 ที่ PPMD 2026