Sarepta Therapeutics Inc(SRPT)
USD --+0.00%
Reward47Moderate
Risk45Moderate
📊75%Data
Thin -32% profit margin · Revenue down 33% YoY
SRPT
+0.0 · +0.00%
USD · NASDAQ
Sarepta Therapeutics Inc | Healthcare
Earnings Deterioration
Market Cap:1.76Bn
ℹ️
Reward Rating
47
Moderate
Bottom 25% (model universe)
75% data coverage
ℹ️
Risk Rating
45
Moderate
Risk Assessment
ℹ️

Educational tool only – Scores are based on historical data and financial metrics for informational purposes. This is not financial advice or a recommendation to buy or sell any security. Always conduct your own research or consult a qualified financial adviser.

ℹ️ Educational tool only · More
Limited data coverage
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Market Performance

Stock returned +10.0% over the past year, broadly in line with market conditions.

Analyst Target

Analyst consensus price target: $21.04.

What is Sarepta Therapeutics Inc?

, a commercial-stage biopharmaceutical company, focuses on the discovery and development of RNA-targeted therapeutics, gene therapies, and other genetic therapeutic modalities for the treatment of rare diseases.

SRPT · Verdict

Moderate reward · moderate risk

SRPT stands out on volatility and balance sheet, but watch the cash flow signal.

Based on 88% data coverage

SRPT · Verdict

What’s working & what to watch

Strengths 2

  • Volatility80/100

    Top decile vs peers

  • Balance sheet73/100

    Current ratio 2.32

Watchouts 2

  • Cash flow16/100

    -16% free-cash-flow margin

  • Profitability32/100

    -32% net margin · -53% ROE

Model-based scoring. For information only — not financial advice.

What is Sarepta Therapeutics Inc?

, a commercial-stage biopharmaceutical company, focuses on the discovery and development of RNA-targeted therapeutics, gene therapies, and other genetic therapeutic modalities for the treatment of rare diseases. It offers EXONDYS 51 injection to treat Duchenne muscular dystrophy (Duchenne) in patients with confirmed mutation of the dystrophin gene that is amenable to exon 51 skipping; VYONDYS 53 for the treatment of Duchenne in patients with confirmed mutation of the dystrophin gene that is amenable to exon 53 skipping; AMONDYS 45 for the treatment of Duchenne in patients with confirmed mutation of the dystrophin gene that is amenable to exon 45 skipping; and ELEVIDYS, an adeno-associated virus based gene therapy for the treatment of ambulatory pediatric patients with Duchenne with a confirmed mutation in the Duchenne gene. The company is listed on the NASDAQ in USA, operating in the Healthcare sector, with a market capitalisation of 1.76B.

Financial Highlights

Investment Breakdown

📈 Growth
Moderate growth momentum — positive trajectory without breakout acceleration.
💰 Profitability
Thin or inconsistent margins weigh on earnings quality.
⚠️ Risk
Risk profile appears balanced versus broad market conditions.
💸 Valuation
Valuation is less clear with a negative earnings base.

OpenBook Logo Analysis

Reward: Moderate (47)

The scoring profile indicates limited reward potential at this time, with growth and momentum offering the most support. Risk indicators are moderate, consistent with typical market exposure.

For informational purposes only. Not financial advice.

Company Information
SectorHealthcare
Market Cap1.76B
P/E RatioN/A
Dividend YieldN/A
52 Week High107.77
52 Week Low10.415
Last AnnualDecember
IPO Date6/3/1997
IncorporatedUSA
Shares Outstanding105M
No. of Employees1,372
IndustryBiotechnology
ExchangeNASDAQ
Beta0.39
CurrencyUSD