Capricor/$CAPR

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About Capricor

Capricor Therapeutics Inc is a clinical-stage biotechnology company focused on the development of transformative cell and exosome-based therapeutics for treating Duchenne muscular dystrophy (DMD), a rare form of muscular dystrophy which results in muscle degeneration and premature death, and other diseases with high unmet medical needs. The company's product pipeline includes CAP-1002, deramiocel an allogeneic cardiac-derived cell therapy. Deramiocel is currently advancing through Phase 3 clinical development for the treatment of Duchenne muscular dystrophy. Through its proprietary StealthXTM platform, the group uses its exosome technology to conduct preclinical research focused on vaccinology, delivering oligonucleotides, proteins, and small molecules to treat.
Ticker
$CAPR
Sector
Health
Primary listing
NASDAQ
Employees
231

Capricor Metrics

BasicAdvanced
$486M
-
-$2.47
0.53
-

What the Analysts think about Capricor

Analyst ratings (Buy, Hold, Sell) for Capricor stock.
Analyst projections of the future price of Capricor stock.

Bulls say / Bears say

HOPE-3 met its primary endpoint, with deramiocel slowing upper-limb decline by 54% versus placebo at 12 months (p=0.03). The results were published in The Lancet after independent peer review, giving the lead programme stronger external validation. (Capricor Therapeutics)
The FDA accepted Capricor’s major BLA amendment and moved the action date to 22 November 2026. The narrower proposed indication focuses on upper-limb function, where HOPE-3 produced its clearest result, while the FDA reviews 24-month follow-up and additional analyses. (Capricor Therapeutics, BioSpace)
Longer-term data could strengthen the case if they confirm durable benefit and tolerability. Capricor has reported five-year HOPE-2 open-label data and is due to present 24-month HOPE-3 results, with 82 of the original 106 patients reaching that time point. (Capricor Therapeutics, Capricor Therapeutics)
The FDA advisory committee voted 9–3 that the available evidence did not support deramiocel’s effectiveness for DMD cardiomyopathy. Although the vote was non-binding and did not cover the proposed upper-limb indication, it is a significant setback for the original regulatory case. (Capricor Therapeutics)
The trial data face regulatory scrutiny over the statistical analysis. Capricor disclosed that the all-patient LVEF result changed from p=0.04 in topline reporting to p=0.09 under the pre-specified model, and that an FDA inspection produced one Form 483 observation. (Capricor Therapeutics)
Capricor remains loss-making and has no approved product revenue to fund operations. Its latest outlook says existing resources cover at least the next twelve months under the current plan, so a regulatory delay or rejection could increase financing needs and dilution risk. (Capricor Therapeutics, Simply Wall St)
Data summarised monthly by Lightyear AI. Last updated on 22 Sept 2026.

Capricor Financial Performance

Revenues and expenses
Income statement
QuarterlyAnnual
Q3 24
QoQ growth
Revenue
Net income
Profit margin

Capricor Earnings Performance

Company profitability
Earnings per share
QuarterlyAnnual
Q4 23
Q1 24
Q2 24
Q3 24
Q4 24
Actual
Expected
Surprise
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