प्राथमिक स्रोत रिकॉर्ड
The Lancet published the full HOPE-3 Phase 3 results, confirming the trial met its primary endpoint with a 54% slowing of upper-limb decline (p=0.03) and cardiac benefit. The peer-reviewed data form the core of the BLA that remains under active FDA review ahead of the August 22, 2026 PDUFA date.
EX-99.1 2 capr-20260729xex99d1.htm EX-99.1 Exhibit 99.1 The Lancet Publishes HOPE-3 Data for Capricor Therapeutics’ Deramiocel in Duchenne Muscular Dystrophy --Independent Peer Review Provides External Validation of the Trial's Design, Statistical Methodology and Findings-- --Randomized, Double-Blind, Placebo-Controlled HOPE-3 Phase 3 Trial (n=106) Met Primary Endpoint, with Deramiocel Slowing Upper Limb Function Decline by 54 Percent versus Placebo (PUL 2.0, p=0.03) and Showing Clinically Meaningful Cardiac Benefit-- --Deramiocel BLA Remains Under Active FDA Review, with PDUFA Target Action Date of August 22, 2026-- SAN DIEGO , July 29, 2026 (GLOBE NEWSWIRE) — Capricor Therapeutics (NASDAQ: CAPR), a biotechnology company developing transformative cell and exosome-based therapeutics for r
कैप्रिकोर पीपीएमडी 2026 में 5-वर्षीय HOPE-2 OLE और HOPE-3 चरण 3 डेटा प्रस्तुत करेगा