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Sarepta Therapeutics (SRPT)
NASDAQ:SRPT

Sarepta Therapeutics (SRPT) AI Stock Analysis

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SRPT

Sarepta Therapeutics

(NASDAQ:SRPT)

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Neutral 48 (OpenAI - 5.2)
Rating:48Neutral
Price Target:
$16.50
▲(0.61% Upside)
Action:ReiteratedDate:03/02/26
The score is primarily constrained by weak financial performance (earnings reversal and persistent cash burn) and bearish technicals (price below all major moving averages with negative MACD). Earnings-call guidance and liquidity are supportive—highlighting a potential 2026 profitability/cash-flow inflection—but near-term commercial and execution uncertainty keeps the overall score below average.
Positive Factors
Cash runway & core cash generation
Nearly $1.0B in cash combined with >$330M of positive base-business cash flow provides multi-quarter funding for R&D, commercialization and operating needs without immediate financing. This runway supports execution on 2026 profitability targets and buffers one-off program charges while management scales commercial efforts.
Durable ELEVIDYS clinical data
Randomized, controlled 3-year data demonstrating sustained, statistically significant functional benefit strengthens long-term clinical credibility and payer/physician confidence. Durable disease-modifying evidence underpins lasting market potential, supports reimbursement discussions and differentiates the therapy versus symptomatic care over multi-year horizons.
Advancing siRNA pipeline
A diversified, multi-program siRNA pipeline spreads clinical and commercial risk beyond DMD and adds multiple mid-term catalysts. Clinical-stage CNS and muscle-targeted assets (DM1, FSHD, Huntington's, SCA2, IPF) create potential new revenue streams and strategic optionality over several years if readouts are positive and facilitate long-term growth and franchise expansion.
Negative Factors
Persistent negative cash flow
Ongoing negative operating and free cash flow signals structural profitability pressure despite revenue gains. Continued cash burn forces reliance on reserves or external financing, risking dilution or higher-cost debt if the planned 2026 cash-flow inflection is delayed, and limits strategic flexibility for capex, launches or acquisitions.
Large inventory & manufacturing charges
Substantial production failures and inventory reserves reveal manufacturing and supply-chain weaknesses that materially depressed margins and earnings. These operational issues can persist, increase unit costs, create recurring period charges, and impair predictability of gross-to-net economics and long-term margin sustainability until production quality stabilizes.
Safety-related uncertainty and dosing pause
Safety incidents eroded prescriber and patient confidence, slowing uptake and complicating label and market restoration efforts. The pause and need for additional prophylaxis data (sirolimus) delays access for non-ambulatory patients, prolongs recovery of peak demand, and heightens regulatory and commercial timing risk across 2026.

Sarepta Therapeutics (SRPT) vs. SPDR S&P 500 ETF (SPY)

Sarepta Therapeutics Business Overview & Revenue Model

Company DescriptionSarepta 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; and VYONDYS 53 for the treatment of duchenne in patients with confirmed mutation of the dystrophin gene that is amenable to exon 53 skipping. The company is also developing AMONDYS 45, a product candidate that uses phosphorodiamidate morpholino oligomer chemistry and exon-skipping technology to skip exon 45 of the dystrophin gene; SRP-5051, a peptide conjugated PMO that binds exon 51 of dystrophin pre-mRNA; SRP-9001, a DMD micro-dystrophin gene therapy program; and SRP-9003, a limb-girdle muscular dystrophies gene therapy program. It has collaboration agreements with F. Hoffman-La Roche Ltd; Nationwide Children's Hospital; Lysogene; Duke University; Genethon; and StrideBio. The company was incorporated in 1980 and is headquartered in Cambridge, Massachusetts.
How the Company Makes MoneySarepta Therapeutics generates revenue primarily through the commercialization of its approved therapies, such as Eteplirsen, which provides a direct sales revenue stream. Additionally, the company engages in partnerships and collaborations with other pharmaceutical companies and research institutions to develop and commercialize its drug candidates. These partnerships often involve upfront payments, milestone payments as products advance through clinical trials, and royalties on future sales. Furthermore, Sarepta may receive funding from grants and research initiatives aimed at advancing its therapeutic pipeline, which contributes to its overall revenue model.

Sarepta Therapeutics Key Performance Indicators (KPIs)

Any
Any
Revenue by Segment
Revenue by Segment
Splits revenue across business lines and markets — for example commercial product sales, collaboration or licensing income, and geographic regions — to reveal where growth is coming from and how diversified the business is. Helps investors see whether Sarepta depends mainly on commercial sales from a small set of drugs, benefits from partner deals or milestone payments, and how exposure to different markets or revenue types affects risk and upside.
Chart InsightsProducts have become the clear revenue engine, showing rapid growth but recent volatility tied to seasonality and shipment disruptions; Collaboration & Other is lumpy and reflects one‑time monetizations that shore up liquidity rather than steady operating income. Management says product demand (ELEVIDYS and the PMO franchise) remains strong despite pauses, but the ESSENCE trial miss and regulatory risk are real near‑term headwinds—successful approval transitions and upcoming siRNA readouts are the key catalysts for sustainable growth.
Data provided by:The Fly

Sarepta Therapeutics Earnings Call Summary

Earnings Call Date:Feb 25, 2026
(Q4-2025)
|
% Change Since: |
Next Earnings Date:May 06, 2026
Earnings Call Sentiment Positive
The call balanced material near-term challenges (safety-related market uncertainty, substantial inventory/manufacturing charges and reported operating losses) with strong underlying positives: robust revenue growth in 2025, a solid cash position, compelling and durable three‑year ELEVIDYS efficacy data, a stable PMO franchise, a rapidly advancing siRNA pipeline with multiple clinical programs and clear 2026 financial guidance. Management emphasized plans to address information deficits, commercial expansion and pipeline milestones; timing risk for ELEVIDYS uptake and non-ambulatory resumption remains notable.
Q4-2025 Updates
Positive Updates
Strong full-year revenue growth
Total revenues for FY2025 were $2.2 billion, up 16% year-over-year, including $1.86 billion in net product revenue (PMOs $966M; ELEVIDYS $899M) showing continued commercial traction.
Solid cash position and positive core cash generation
Ended 2025 with $954 million in cash and investments (up $89M in Q4); base business (ex-Arrowhead payments) generated more than $330 million of positive cash flow in 2025 and management expects to be cash-flow positive and non-GAAP profitable in 2026 under reasonable scenarios.
ELEVIDYS durable, disease-modifying data (EMBARK 3-year)
Three-year EMBARK Part 1 results show durable, statistically significant efficacy vs external control: 73% slowing in disease progression for time-to-rise, 70% for 10m walk/run, NSAA +4.39 point difference at year 3 (p=0.0002); no new safety signals reported through three years.
PMO franchise stability and compliance
PMO net product revenue totaled $966 million in 2025; Q4 PMO revenue $259 million (EXONDYS $148M, VYONDYS $34M, AMONDYS $77M) with year-after-year compliance rates consistently over 90%.
Pipeline advancement: multiple clinical-stage siRNA programs
Five clinical-stage siRNA programs advancing (DM1 SRP-1003, FSHD, IPF, SCA2, Huntington's SRP-1005 initiated), with additional preclinical programs (SCA1, SCA3) and planned readouts (preliminary DM1/FSHD data end of quarter; further PD/splice data later in 2026).
Regulatory and commercial milestones
ELEVIDYS received traditional approval for ambulatory patients and approval to run a sirolimus pretreatment study for non-ambulatory patients; meeting with FDA scheduled to discuss transitioning AMONDYS and VYONDYS to traditional approval following ESSENCE confirmatory data.
2026 revenue and collaboration visibility
Provided net product revenue guidance for 2026 of $1.2B–$1.4B (management advises modeling toward the low end given timing uncertainty) and expects collaboration, contract manufacturing, and royalty revenues of $450M–$550M in 2026 (including a $40M Roche milestone and ~$325M noncash collaboration revenue).
Negative Updates
Safety-related events and market uncertainty in 2025
Unanticipated tragic safety events in 2025 created short-lived FDA actions and patient/physician hesitation that reshaped perceptions of gene therapy and reduced near-term ELEVIDYS uptake; company views 2026 as a 'reset' year to address the information deficit.
Significant inventory and manufacturing charges
Q4 cost of sales included a $193 million charge ( $165M noncash excess inventory reserve + $28M purchase commitment cancellation fees) after a raw material and purchase-commitment review; full-year cost of sales were $840M with nearly half reflecting failed production batches, inventory reserves and related period charges.
Reported GAAP and non-GAAP operating losses
FY2025 GAAP operating loss was $700 million and non-GAAP operating loss was $492 million; after adjustments management stated the underlying business would have shown positive operating profit ($226M GAAP / $391M non‑GAAP) excluding restructuring and Arrowhead transaction expenses.
Near-term revenue timing uncertainty and Q1 softness
Management expects Q1 revenue to be about flat to down up to 15% versus prior quarter; six planned ELEVIDYS infusions were rescheduled into 2026 (Q4 ELEVIDYS revenue was $110M, impacted by a severe flu season and the reschedules), and long enrollment-to-infusion cycles mean commercial initiatives likely won’t materially lift revenue until H2 2026 or beyond.
Non-ambulatory dosing paused pending sirolimus results
Non-ambulatory commercial dosing was paused after 155 non-ambulatory patients were treated through July 2025; Cohort 8 (sirolimus prophylaxis) is enrolling ~25 participants with results expected by end of 2026 — resumption of routine non-ambulatory dosing depends on those outcomes and further FDA discussions.
Margins pressured but expected to normalize
Excluding inventory and batch-related charges, unit sales-driven gross margins were in the low-80% range for 2025; management expects 2026 unit margins to be in the high-70% range as production volumes decline and fewer period charges are expected.
Company Guidance
Sarepta gave broad 2026 financial guidance and key metrics: net product revenue of $1.2–$1.4 billion (Q1 expected about flat to down ~15% vs. prior quarter), 2026 non‑GAAP R&D+SG&A of $800–$900 million, and the company expects to be cash‑flow positive and non‑GAAP profitable in 2026 under reasonable scenarios. They closed 2025 with $954 million cash & investments (up $89 million in Q4) and base business positive cash flow >$330 million ex‑Arrowhead; full‑year 2025 results were $2.2 billion total revenue (+16% YoY) including $1.86 billion net product revenue ($966M PMO franchise, $899M ELEVIDYS) and $334 million collaboration/CM/royalty revenue. Q4 detail: PMO net product revenue $259M (EXONDYS $148M, VYONDYS $34M, AMONDYS $77M) and ELEVIDYS $110M (impacted by a severe flu season and six rescheduled infusions); Q4 cost of sales $399M (including a $193M charge — $165M noncash inventory reserve + $28M purchase‑commitment fees), FY COS $840M. For 2026 they expect collaboration/CM/royalty revenue of $450–$550M (including a $40M Roche Q1 milestone and ~$325M noncash collaboration revenue tied to Roche), project unit margins in the high‑70% range for 2026 (2025 unit margins were low‑80% excluding period charges), and note balance‑sheet actions that refinanced $291M of 2027 notes into 2030 leaving a $159M remaining stub.

Sarepta Therapeutics Financial Statement Overview

Summary
Weighed down by deteriorating TTM profitability (net margin -38.3% with negative EBIT/EBITDA) and ongoing cash burn (negative operating and free cash flow, with TTM FCF down 18.4% YoY). Offsetting factors include strong gross margin (~61%) and an improved leverage profile (debt-to-equity ~0.17), but sustained losses and cash outflows remain the key risk.
Income Statement
43
Neutral
TTM (Trailing-Twelve-Months) results show a sharp deterioration: revenue declined 8.9% and profitability swung to sizable losses (net margin -38.3%, with negative EBIT and EBITDA margins). This is a meaningful reversal from 2024, which delivered positive operating profit and a 12.4% net margin. A clear positive is consistently strong gross profitability (TTM gross margin ~61%), but the cost structure and/or charges below gross profit are pressuring earnings power and make near-term profitability less predictable.
Balance Sheet
62
Positive
Leverage looks manageable in TTM (Trailing-Twelve-Months), with debt-to-equity at ~0.17 and equity of ~$1.14B against ~$3.35B of assets—an improvement versus the more levered 2022–2024 period (debt-to-equity peaked above 4.2 in 2022). The key weakness is returns: TTM (Trailing-Twelve-Months) losses drive deeply negative return on equity, and equity can be vulnerable if losses persist. Overall, the balance sheet appears less debt-burdened than recent history, but profitability needs to stabilize to protect capital.
Cash Flow
35
Negative
Cash generation remains a concern: operating cash flow and free cash flow are negative in both TTM (Trailing-Twelve-Months) and 2024, with TTM free cash flow down 18.4% year over year. While free cash flow is mathematically higher than net income due to non-cash items (free cash flow to net income > 1), the underlying reality is ongoing cash burn, implying continued reliance on cash reserves or financing unless operating performance improves. The only clear bright spot in the history provided is 2020, when operating and free cash flow were positive, but that has not been sustained.
BreakdownDec 2025Dec 2024Dec 2023Dec 2022Dec 2021
Income Statement
Total Revenue2.20B1.90B1.24B933.01M701.89M
Gross Profit1.32B1.58B1.09B793.02M604.84M
EBITDA-647.97M316.89M-453.69M-594.85M-317.41M
Net Income-713.41M235.24M-535.98M-703.49M-418.78M
Balance Sheet
Total Assets3.35B3.96B3.26B3.13B3.15B
Cash, Cash Equivalents and Short-Term Investments939.65M1.35B1.68B1.99B2.12B
Total Debt1.04B1.34B1.40B1.62B1.15B
Total Liabilities2.21B2.44B2.41B2.74B2.22B
Stockholders Equity1.14B1.53B859.34M384.95M928.01M
Cash Flow
Free Cash Flow-307.45M-352.74M-588.34M-357.60M-481.66M
Operating Cash Flow-205.48M-205.79M-500.99M-325.35M-443.17M
Investing Cash Flow69.64M755.56M-165.80M-1.05B495.41M
Financing Cash Flow-168.34M124.81M125.00M232.51M561.57M

Sarepta Therapeutics Technical Analysis

Technical Analysis Sentiment
Negative
Last Price16.40
Price Trends
50DMA
19.50
Negative
100DMA
20.12
Negative
200DMA
20.68
Negative
Market Momentum
MACD
-0.70
Negative
RSI
38.89
Neutral
STOCH
55.39
Neutral
Evaluating momentum and price trends is crucial in stock analysis to make informed investment decisions. For SRPT, the sentiment is Negative. The current price of 16.4 is below the 20-day moving average (MA) of 17.46, below the 50-day MA of 19.50, and below the 200-day MA of 20.68, indicating a bearish trend. The MACD of -0.70 indicates Negative momentum. The RSI at 38.89 is Neutral, neither overbought nor oversold. The STOCH value of 55.39 is Neutral, not indicating any strong overbought or oversold conditions. Overall, these indicators collectively point to a Negative sentiment for SRPT.

Sarepta Therapeutics Risk Analysis

Sarepta Therapeutics disclosed 65 risk factors in its most recent earnings report. Sarepta Therapeutics reported the most risks in the "Tech & Innovation" category.
Finance & Corporate - Financial and accounting risks. Risks related to the execution of corporate activity and strategy
Latest Risks Added 0 New Risks

Sarepta 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
70
Outperform
$2.06B6.20-76.45%45.38%92.85%
63
Neutral
$2.82B-228.91-10.26%129.21%80.35%
56
Neutral
$2.96B-5.63-61.45%-2.75%
51
Neutral
$7.86B-0.30-43.30%2.27%22.53%-2.21%
49
Neutral
$1.90B-18.31%191.53%5.09%
49
Neutral
$5.52B-5.86-100.22%4.32%
48
Neutral
$1.72B-3.16-57.52%47.15%-311.26%
* Healthcare Sector Average
Performance Comparison
Ticker
Company Name
Price
Change
% Change
SRPT
Sarepta Therapeutics
16.40
-84.95
-83.82%
BCRX
BioCryst
8.22
0.48
6.20%
MESO
Mesoblast
14.55
1.36
10.31%
COGT
Cogent Biosciences
34.00
26.61
360.08%
ARQT
Arcutis Biotherapeutics
22.75
6.33
38.55%
DYN
Dyne Therapeutics
17.92
5.61
45.57%

Sarepta Therapeutics Corporate Events

Business Operations and StrategyExecutive/Board Changes
Sarepta Therapeutics Announces Planned CEO Leadership Transition
Neutral
Feb 25, 2026

On February 25, 2026, Sarepta Therapeutics said Chief Executive Officer Douglas Ingram notified the company of his decision to retire by the end of 2026 or when a successor is appointed. The board has begun searching both internal and external candidates, signaling a planned leadership transition that may shape Sarepta’s strategic direction and execution over the coming years.

The most recent analyst rating on (SRPT) stock is a Hold with a $17.00 price target. To see the full list of analyst forecasts on Sarepta Therapeutics stock, see the SRPT Stock Forecast page.

Business Operations and StrategyPrivate Placements and Financing
Sarepta Therapeutics Extends Debt Maturities with New Notes
Positive
Dec 19, 2025

On December 10, 2025, Sarepta Therapeutics, Inc. entered into privately negotiated exchange agreements with certain holders of its 1.25% Convertible Senior Notes due 2027, including an entity affiliated with board member Michael Chambers, to exchange approximately $291.4 million in principal of the existing notes for an equal principal amount of new 4.875% Convertible Senior Notes due 2030 plus about $31.6 million in cash. The new notes were issued on December 18, 2025, under an existing indenture and form part of the same series as the $602.0 million of 4.875% Convertible Senior Notes due 2030 issued in August 2025, bringing the total outstanding principal of that 2030 series to approximately $893.4 million and effectively extending the company’s debt maturity profile while modestly increasing its cash outlay to participating noteholders.

The most recent analyst rating on (SRPT) stock is a Hold with a $17.00 price target. To see the full list of analyst forecasts on Sarepta Therapeutics stock, see the SRPT Stock Forecast page.

Private Placements and Financing
Sarepta Therapeutics Refinances Convertible Senior Notes
Neutral
Dec 11, 2025

On December 10, 2025, Sarepta Therapeutics entered into exchange agreements to refinance approximately $291.4 million of its 1.25% Convertible Senior Notes due 2027. These notes will be exchanged for new 4.875% Convertible Senior Notes due 2030 and approximately $31.6 million in cash. The exchange aims to enhance the company’s financial structure by consolidating its debt under a new series of notes, increasing the total principal amount of the 2030 notes to $893.4 million. This move could influence the market price of Sarepta’s common stock and notes, as the placement agent plans to purchase shares in privately negotiated transactions.

The most recent analyst rating on (SRPT) stock is a Buy with a $37.00 price target. To see the full list of analyst forecasts on Sarepta Therapeutics stock, see the SRPT Stock Forecast page.

Executive/Board Changes
Sarepta Grants CEO Equity Awards After Eight Years
Neutral
Dec 8, 2025

On December 7, 2025, Sarepta Therapeutics‘ Board of Directors granted equity awards to CEO Douglas S. Ingram under the company’s 2018 Equity Incentive Plan. This marks the first equity grant for Mr. Ingram since 2017, with the award divided equally between time-based restricted stock units and performance-based awards, each valued at approximately $6 million. The performance-based portion is contingent on the company’s Incentive EBITDA performance over a two-year period, potentially doubling in value if targets are met, and is subject to Mr. Ingram’s continued service.

The most recent analyst rating on (SRPT) stock is a Hold with a $21.00 price target. To see the full list of analyst forecasts on Sarepta Therapeutics stock, see the SRPT Stock Forecast page.

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: Mar 02, 2026