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Capricor Therapeutics (CAPR)
NASDAQ:CAPR
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Capricor Therapeutics (CAPR) AI Stock Analysis

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CAPR

Capricor Therapeutics

(NASDAQ:CAPR)

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Neutral 45 (OpenAI - Gpt-5.6Sol)
Rating:45Neutral
Price Target:
$5.50
▼(-33.66% Downside)
Action:Reiterated
Date:10/22/26
The score is primarily pressured by weak financial performance (no TTM revenue, ongoing losses, and sustained cash burn) and bearish technicals (price below key moving averages with negative MACD). Valuation provides limited insight due to negative earnings and no dividend, while the earnings call adds a balanced but risk-heavy outlook—strong primary endpoint and cash position, yet meaningful regulatory uncertainty and rising expenses.
Positive Factors
Clinical efficacy
The statistically significant HOPE-3 primary endpoint provides substantive clinical support for deramiocel’s refined upper-limb indication. Peer-reviewed and trial-backed efficacy can strengthen the regulatory case, differentiate the lead program, and support future commercial adoption if approval is secured.
Negative Factors
Regulatory delay
The major-amendment classification and three-month PDUFA extension lengthen the path to a commercial decision and increase execution uncertainty. Delayed approval postpones potential product revenue, keeps development spending elevated, and requires management to sustain regulatory momentum for longer.
Read all positive and negative factors
Positive Factors
Negative Factors
Clinical efficacy
The statistically significant HOPE-3 primary endpoint provides substantive clinical support for deramiocel’s refined upper-limb indication. Peer-reviewed and trial-backed efficacy can strengthen the regulatory case, differentiate the lead program, and support future commercial adoption if approval is secured.
Read all positive factors

Capricor Therapeutics (CAPR) vs. SPDR S&P 500 ETF (SPY)

Capricor Therapeutics Business Overview & Revenue Model

Company Description
Capricor Therapeutics, Inc. is a clinical-stage biotechnology company, which focuses on the development of transformative cell and exosome-based therapeutics for treating Duchenne muscular dystrophy (“DMD”), a rare form of muscular dystrophy which...
How the Company Makes Money
As a clinical-stage biotechnology company, Capricor has historically generated little to no recurring revenue from product sales because its lead candidates have been in development and not broadly commercialized. When revenue is present, it is ty...

Capricor Therapeutics Earnings Call Summary

Earnings Call Date:Aug 13, 2026
(Q2-2026)
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% Change Since: |
Next Earnings Date:Nov 17, 2026
Earnings Call Sentiment Neutral
The call balanced meaningful clinical and regulatory progress (Lancet publication, statistically significant primary HOPE‑3 endpoint for upper limb function, established safety exposure, operational in‑house manufacturing and $237.9M cash) against substantial near‑term challenges (AdCom vote against the cardiomyopathy question, mixed secondary endpoint results, no revenue, rising operating expenses and widening losses, a Form 483 observation, paused non‑Daramycin pipeline work, and an ongoing commercial dispute with NS Pharma). Management has a clear path to submit an amendment focused on the primary skeletal muscle indication and the FDA indicated willingness to review it, but regulatory and financial risks remain in the near term.
Positive Updates
Regulatory Path Forward and PDUFA Timeline
BLA for Daramycin under FDA review with current PDUFA action date of August 22, 2026; company plans to submit a BLA amendment including 24-month open‑label extension data to pursue a refined upper‑limb skeletal muscle indication and FDA indicated willingness to review the amendment and extend the PDUFA date.
Negative Updates
Advisory Committee Vote Against Cardiomyopathy Indication
FDA Cellular, Tissue and Gene Therapies Advisory Committee voted 3 in favor, 9 against (0 abstentions) on whether available evidence provides substantial evidence of effectiveness for cardiomyopathy in DMD — a significant setback for the originally requested cardiomyopathy indication.
Read all updates
Q2-2026 Updates
Negative
Regulatory Path Forward and PDUFA Timeline
BLA for Daramycin under FDA review with current PDUFA action date of August 22, 2026; company plans to submit a BLA amendment including 24-month open‑label extension data to pursue a refined upper‑limb skeletal muscle indication and FDA indicated willingness to review the amendment and extend the PDUFA date.
Read all positive updates
Company Guidance
Management said the Daramycin BLA remains under FDA review with a current PDUFA target action date of August 22, 2026 and noted an FDA advisory committee vote of 3–9 against approval for the cardiomyopathy indication; they plan to submit a BLA amendment (timing being finalized) that adds 24‑month open‑label extension data and additional analyses, after which the FDA has indicated it may extend the PDUFA date. They highlighted HOPE‑3 results showing a statistically significant primary upper‑limb (PUL 2.0) benefit — a 4.5% mean treatment difference (1.2 absolute change), p=0.029 — and key secondary left ventricular ejection fraction effects of 2.4 percentage points (p=0.04) on top‑line, 1.8 points (p=0.09) under the prespecified model, and a cardiomyopathy subgroup result of 2.8 points (p=0.02). The program has delivered ~1,300 IV infusions across >200 patients in 3 trials, >80 patients in open‑label extensions (some on continuous infusions >5 years), and the Phase 3 data were published in The Lancet; FDA BIMO inspection yielded one Form 483 to which the company has responded. Financially, Capricor had $237.9M in cash, cash equivalents and marketable securities as of 6/30/2026, reported no revenue in Q2 2026 or Q2 2025, Q2 operating expenses of $42.9M (vs $27.7M year‑ago), Q2 net loss of ~$40.7M ($0.70/share) (vs ~$25.9M, $0.57/share), six‑month net loss of $74.7M (vs $50.3M), and an accumulated deficit of ~$379.6M; commercial launch planning is being paced, the in‑house GMP facility in San Diego is operational, and second‑floor expansion validation/approval is estimated in 2027, while arbitration with NS Pharma is expected to begin this fall.

Capricor Therapeutics Financial Statement Overview

Summary
Financials reflect a high-risk, cash-burning biotech profile: persistent operating and net losses across multiple years, zero TTM revenue, and consistently negative operating/free cash flow. The balance sheet is a partial offset with meaningful equity and debt-to-equity below ~0.4, but debt rose sharply in TTM and negative returns persist. The unusual TTM EBITDA turning positive while EBIT and net income remain deeply negative also raises earnings-quality concerns.
Income Statement
18
Very Negative
Balance Sheet
56
Neutral
Cash Flow
24
Negative
BreakdownTTMDec 2025Dec 2024Dec 2023Dec 2022Dec 2021
Income Statement
Total Revenue0.000.0022.27M25.18M2.55M244.90K
Gross Profit-20.36M0.00-27.70M-11.27M-19.27M244.90K
EBITDA1.17B-100.11M-39.04M-21.22M-28.49M-19.78M
Net Income-129.42M-105.04M-40.47M-22.29M-29.02M-20.02M
Balance Sheet
Total Assets368.74M355.95M170.48M58.73M50.09M41.33M
Cash, Cash Equivalents and Short-Term Investments237.93M318.13M151.52M39.49M41.42M34.89M
Total Debt91.05M17.94M4.83M5.61M5.94M6.25M
Total Liabilities122.52M50.16M25.02M36.13M38.31M9.96M
Stockholders Equity246.22M305.79M145.46M22.60M11.79M31.37M
Cash Flow
Free Cash Flow-129.78M-72.72M-41.53M-27.64M1.56M-18.01M
Operating Cash Flow-104.00M-69.81M-40.00M-25.60M4.92M-16.81M
Investing Cash Flow-144.36M97.48M-116.18M5.11M-35.07M-1.20M
Financing Cash Flow246.05M248.89M152.77M25.58M4.87M20.23M

Capricor Therapeutics Technical Analysis

Technical Analysis Sentiment
Negative
Last Price8.29
Price Trends
50DMA
8.15
Negative
100DMA
13.41
Negative
200DMA
21.14
Negative
Market Momentum
MACD
-0.72
Positive
RSI
33.75
Neutral
STOCH
9.84
Positive
Evaluating momentum and price trends is crucial in stock analysis to make informed investment decisions. For CAPR, the sentiment is Negative. The current price of 8.29 is above the 20-day moving average (MA) of 7.51, above the 50-day MA of 8.15, and below the 200-day MA of 21.14, indicating a bearish trend. The MACD of -0.72 indicates Positive momentum. The RSI at 33.75 is Neutral, neither overbought nor oversold. The STOCH value of 9.84 is Positive, not indicating any strong overbought or oversold conditions. Overall, these indicators collectively point to a Negative sentiment for CAPR.

Capricor Therapeutics Risk Analysis

Capricor Therapeutics disclosed 31 risk factors in its most recent earnings report. Capricor Therapeutics reported the most risks in the "Finance & Corporate" category.
Finance & Corporate - Financial and accounting risks. Risks related to the execution of corporate activity and strategy
Latest Risks Added 0 New Risks

Capricor Therapeutics Peers Comparison

Overall Rating
UnderperformOutperform
Sector (51)
Financial Indicators
Name
Overall Rating
Market Cap
P/E Ratio
ROE
Dividend Yield
Revenue Growth
EPS Growth
51
Neutral
$7.86B-0.30-43.30%2.27%22.53%-2.21%
48
Neutral
$251.61M-3.88-41.69%―6280.00%-212.54%
48
Neutral
$229.85M-2.43-41.85%――64.51%
45
Neutral
$344.76M-2.42-56.60%―-100.00%-49.28%
45
Neutral
$251.38M-14.31-5.76%――93.45%
44
Neutral
$440.97M-1.76-220.07%―12.00%-9.21%
41
Neutral
$634.77M-3.10-72.28%――31.81%
* Healthcare Sector Average
Performance Comparison
Ticker
Company Name
Price
Change
% Change
CAPR
Capricor Therapeutics
5.93
-0.25
-4.05%
RCKT
Rocket Pharmaceuticals
2.29
-1.65
-41.88%
ABEO
Abeona Therapeutics
4.40
-1.14
-20.58%
RGNX
RegenXBio
6.68
-6.94
-50.95%
SLDB
Solid Biosciences
5.92
0.02
0.34%
LXEO
Lexeo Therapeutics, Inc.
2.80
-7.04
-71.54%

Capricor Therapeutics Corporate Events

Business Operations and StrategyProduct-Related AnnouncementsRegulatory Filings and Compliance
Capricor Therapeutics Faces FDA Delay for Deramiocel Review
Negative
Aug 24, 2026
On August 24, 2026, Capricor Therapeutics announced that the U.S. Food and Drug Administration extended the Prescription Drug User Fee Act target action date for its Biologics License Application for Deramiocel, an investigational cell therapy for...
Business Operations and StrategyRegulatory Filings and Compliance
Capricor Faces FDA Panel Setback on Deramiocel Therapy
Negative
Jul 30, 2026
On July 29, 2026, the FDA’s Cellular, Tissue and Gene Therapies Advisory Committee concluded that current evidence does not support the effectiveness of Capricor Therapeutics‘ Deramiocel for treating cardiomyopathy in Duchenne muscular...
Business Operations and StrategyProduct-Related AnnouncementsRegulatory Filings and Compliance
Lancet Validates Capricor’s HOPE-3 Duchenne Trial Results
Positive
Jul 29, 2026
On July 29, 2026, Capricor reported that The Lancet published the final one-year results from its Phase 3 HOPE-3 trial of Deramiocel in Duchenne muscular dystrophy, confirming the study met its primary endpoint with a 54% slowing of upper limb fun...
Glossary
BuyA stock rated as a "Buy" is expected to perform better than the overall market or a specific benchmark over the near-to-medium term. This rating suggests the stock is likely to deliver higher returns compared to other stocks in the same sector or market index. Note: This is not investment advice; please consult a financial advisor before making investment decisions.
HoldA stock rated as a "Hold" is expected to perform in line with the overall market or a specific benchmark. This rating indicates that the stock is neither particularly compelling nor unfavorable for investment. Note: This is not investment advice; please consult a financial advisor before making investment decisions.
SellA stock rated as a "Sell" is expected to perform worse than the overall market or a specific benchmark over the near-to-medium term. This rating suggests the stock may deliver lower returns compared to other stocks in the same sector or market index. Note: This is not investment advice; please consult a financial advisor before making investment decisions.

Disclaimer

This AI Analyst Stock Report is automatically generated by our AI systems using advanced algorithms and publicly available financial, technical, and market data. While the information provided aims to be accurate and insightful, it is intended for informational purposes only and should not be considered financial advice. Any content created by an AI (Artificial Intelligence) system may contain inaccuracies and/or contain errors. Investing in stocks carries inherent risks, and past performance is not indicative of future results. This report does not account for your personal financial circumstances, objectives, or risk tolerance. Always conduct your own research or consult with a qualified financial advisor before making investment decisions. The analysis and recommendations provided are based on historical and current data and may not fully reflect future market conditions or unexpected developments. Neither the creators of this report nor its affiliated entities guarantee the accuracy, completeness, or reliability of the information presented. Use this report at your own discretion and risk.Date of analysis: Oct 22, 2026