Sarepta Therapeutics Inc.(0L35)
USD --+0.00%
Reward54Moderate
Risk54Moderate
📊75%Data
Thin -32% profit margin · Revenue down 33% YoY
0L35
+0.0 · +0.00%
USD · LSE
Sarepta Therapeutics Inc. |
Earnings Deterioration
Market Cap:
ℹ️
Reward Rating
54
Moderate
Bottom 50% (model universe)
75% data coverage
ℹ️
Risk Rating
54
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.

What is Sarepta Therapeutics Inc.?

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

0L35 · Verdict

Moderate reward · elevated risk

0L35 stands out on volatility and valuation, but watch the cash flow signal.

Based on 88% data coverage

0L35 · Verdict

What’s working & what to watch

Strengths 2

  • Volatility95/100

    Top decile vs peers

  • Valuation67/100

    Above average

Watchouts 3

  • Cash flow16/100

    -14% free-cash-flow margin

  • Profitability32/100

    -32% net margin · -53% ROE

  • Balance sheet43/100

    Current ratio 2.32

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, siRNA platform, gene therapy, and other genetic therapeutic modalities for the treatment of rare diseases. It offers EXONDYS 51 for the treatment of Duchenne in patients who have a confirmed mutation of the dystrophin gene that is amenable to exon 51 skipping; VYONDYS 53 for the treatment of Duchenne in patients who have a confirmed mutation of the dystrophin gene that is amenable to exon 53 skipping; AMONDYS 45 for the treatment of Duchenne in patients who have a confirmed mutation of the dystrophin gene that is amenable to exon 45 skipping; and ELEVIDYS, an AAV-based gene therapy, which is contraindicated in patients with any deletion in exon 8 and/or exon 9 in the Duchenne gene. The company is listed on the LSE in UK.

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 (54)

The scoring profile indicates limited reward potential at this time, with valuation and growth offering the most support. Risk indicators are elevated — volatility and macro sensitivity warrant consideration.

For informational purposes only. Not financial advice.

Company Information
SectorN/A
Market CapN/A
P/E RatioN/A
Dividend YieldN/A
52 Week High63.9829
52 Week Low10.485
Last AnnualDecember
IPO DateN/A
IncorporatedUK
Shares Outstanding67M
No. of Employees835
IndustryN/A
ExchangeLSE
Beta0.283
CurrencyUSD