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Sarepta Therapeutics/$SRPT

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About Sarepta Therapeutics

Sarepta Therapeutics Inc is a commercial-stage biopharmaceutical company focused on the discovery and development of RNA-targeted therapies, gene therapies, and other genetic medicines for rare diseases, particularly neuromuscular disorders. The company has developed approved treatments for Duchenne muscular dystrophy, including EXONDYS 51, VYONDYS 53, AMONDYS 45, and ELEVIDYS, and is advancing additional therapeutic candidates for neuromuscular and other rare diseases. The company operates in one segment: discovering, developing, manufacturing, and delivering therapies to patients with rare diseases.
Ticker
$SRPT
Sector
Health
Primary listing
NASDAQ
Employees
835

SRPT Metrics

BasicAdvanced
$1.9B
-
-$1.09
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What the Analysts think about SRPT

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

Bulls say / Bears say

A two-year analysis of 25 ambulatory patients aged 8–12 found better motor-function measures than matched external controls, extending the efficacy case into older patients. The comparison was not randomised, so the findings still need confirmation. (BioSpace)
The established PMO franchise generated $230.6 million in Q2 net product sales, while Sarepta reported $13.3 million in GAAP operating income and $945 million in cash, restricted cash and investments. This commercial base helps fund the company’s development programmes. (Sarepta Therapeutics)
Phase 1/2 multiple-ascending-dose readouts for FSHD and DM1 remained on track for the second half of 2026, and dosing had begun in Sarepta’s first-in-human Huntington’s study. These programmes offer potential growth beyond Duchenne, although they are still early-stage. (Sarepta Therapeutics)
ELEVIDYS net product sales fell to $98.1 million in Q2 from $281.9 million a year earlier after its label was restricted to ambulatory patients. Sarepta also narrowed its 2026 net product revenue guidance to $1.2–$1.3 billion, signalling continued commercial pressure. (Sarepta Therapeutics)
A second non-ambulatory patient reportedly died from acute liver failure after receiving ELEVIDYS, prompting a pause in commercial dosing for non-ambulatory patients and in the ENvision confirmatory trial. The renewed safety concern could hinder any effort to restore broader use. (Center for Genetics and Society)
Amondys 45 and Vyondys 53 failed to significantly improve motor function versus placebo in their ESSENCE confirmatory trial. Although the FDA accepted applications to convert them to traditional approval, the trial result leaves a key efficacy question unresolved ahead of the 2027 decisions. (BioSpace)
Data summarised monthly by Lightyear AI. Last updated on 1 Nov 2026.

SRPT Financial Performance

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

SRPT Earnings Performance

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

Funds containing SRPT

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