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Capricor Therapeutics (CAPR) investor relations material

Capricor Therapeutics Study Result summary

Complete event summary combining all related documents: earnings call transcript, report, and slide presentation.
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Study Result summary17 Dec, 2025

Study background and design

  • HOPE-3 is a phase III, randomized, double-blind, placebo-controlled trial evaluating Deramiocel for Duchenne muscular dystrophy (DMD).

  • 106 patients were randomized; 105 received treatment, with balanced demographics and most being non-ambulatory.

  • The primary endpoint was the Performance of the Upper Limb (PUL) 2.0; key secondary endpoints included cardiac MRI measures and patient-reported outcomes.

  • The trial included both late ambulatory and non-ambulatory patients, targeting those at high risk for upper limb and cardiac function loss.

  • Deramiocel is a cell therapy with anti-fibrotic, immunomodulatory, and anti-inflammatory mechanisms.

Efficacy results

  • Deramiocel showed a 54% slowing of upper limb deterioration compared to placebo, achieving statistical significance (p=0.029).

  • Cardiac function, measured by left ventricular ejection fraction (LVEF), showed a 91% slowing of disease progression in treated patients.

  • Patients with pre-existing cardiomyopathy had even greater benefit, with over a 3 percentage point difference in LVEF compared to placebo.

  • All Type I error-controlled secondary endpoints, including mid-level PUL, global statistical test, and late gadolinium enhancement (cardiac scar), reached statistical significance.

  • Improvements were observed in both skeletal muscle and cardiac function, with Deramiocel potentially being first-in-class for DMD cardiomyopathy.

Safety and tolerability

  • Deramiocel was generally well tolerated; most adverse events were mild or moderate and resolved within 24 hours.

  • Only one serious adverse event occurred in the treatment arm, resolving without sequelae; the placebo arm had five serious events.

  • A pretreatment protocol with steroids and antihistamines was implemented to prevent infusion reactions.

  • Long-term safety data from the HOPE-2 open-label extension (over four years) showed no new safety concerns.

  • Infusions are administered quarterly at medical centers, not suitable for home infusion.

What is the anticipated FDA review timeline?
How does deramiocel differ from existing DMD therapies?
What are the plans for Becker cardiomyopathy?
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Q4 202527 Feb, 2026
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Capricor Therapeutics, Inc., a clinical-stage biotechnology company, focuses on the development of transformative cell and exosome-based therapeutics for the treatment and prevention of spectrum of diseases and disorders.

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