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
$2.2B
-
-$1.32
0.26
-

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

Sarepta generated $328.7 million of product revenue in Q2 2026, including $98.1 million from ELEVIDYS, demonstrating that the company retains meaningful commercial traction despite the gene therapy’s safety overhang. (Q2 2026 Results)
Sarepta held $945.0 million in cash, cash equivalents, restricted cash, and investments as of June 30, 2026, providing substantial liquidity to fund operations and advance its pipeline while limiting near-term financing pressure. (SEC Form 10-Q)
The FDA accepted Sarepta’s supplemental applications for VYONDYS 53 and AMONDYS 45 for filing in June 2026, preserving a potential regulatory and commercial catalyst for the company’s established exon-skipping portfolio. (SEC Form 10-Q)
ELEVIDYS remains commercially unavailable for non-ambulatory Duchenne patients while Sarepta seeks FDA agreement on whether sirolimus data can support resuming dosing, leaving a major population and regulatory outcome uncertain. (SEC Form 10-Q)
Sarepta disclosed that the ESSENCE confirmatory trial for VYONDYS 53 and AMONDYS 45 failed to achieve statistical significance on its primary endpoint, creating risk for the durability and labeling of its exon-skipping franchise. (SEC Form 10-Q)
Regenxbio and the University of Pennsylvania filed patent litigation alleging that Sarepta’s AAV gene-therapy manufacturing process infringes their cultured-host-cell technology patents, creating potential legal costs, royalties, or operational constraints. (SEC Form 10-Q)
Data summarised monthly by Lightyear AI. Last updated on 8 Sept 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

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