Capricor Therapeutics

its lead asset Deramiocel (formerly CAP-1002), an allogeneic cardiosphere-derived cell therapy whose benefit in Duchenne muscular dystrophy is believed to work partly through paracrine exosome secretion, has a Biologics License Application now scheduled for FDA Advisory Committee review on July 29, 2026,…

Country
United States
Ticker
CAPR
cell-therapy us
Coverage
CNEUUS
regenerative-personalized
Regulatorsfdaemanmpa

Verifiable facts

FactValueSource
Funding$278.6 million in cash, cash equivalents and marketable securities as of March 31, 2026biospace.com · capricor.com
CapacityScaling to approximately 2,000–2,500 patients per year or 10,000 doses annually at full capacity upon validationbiospace.com · capricor.com
CertificationGMP compliant manufacturing facility in San Diego successfully completed an FDA Pre-License Inspectionbiospace.com · capricor.com · sec.gov
Regulatory approvalDeramiocel has Orphan Drug, RMAT, ATMP, and Rare Pediatric Disease designations; BLA under FDA review with PDUFA date of August 22, 2026biospace.com · capricor.com · sec.gov
Production siteGMP manufacturing facility in San Diego, Californiabiospace.com · capricor.com
HeadcountApproximately 247-299 employees as of mid-2026 medium confidencealtindex.com · finance.yahoo.com
Revenue$0 revenue for the first quarter of 2026 and for the full year 2025biospace.com · capricor.com

Independent sources: altindex.com · biospace.com · finance.yahoo.com · sec.gov

Technologies
NameClusterRisk
Exosome therapy & extracellular vesiclesregenerative-personalizedHigh

Compiled by BIOECON from primary sources.

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