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Sarepta Therapeutics Stock Price

Symbol: NasdaqGS:SRPTMarket Cap: US$1.6bCategory: Pharmaceuticals & Biotech

SRPT Share Price Performance

US$15.91
-124.74 (-88.69%)
81.1% undervalued intrinsic discount
US$84.18
Fair Value
US$15.91
-124.74 (-88.69%)
81.1% undervalued intrinsic discount
US$84.18
Fair Value
Price US$15.91
AnalystHighTarget US$84.18
AnalystLowTarget US$70.00
AnalystConsensusTarget US$21.80

SRPT Community Narratives

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AnalystHighTarget
AnalystHighTarget·Updated
Fair Value US$84.18 81.1% undervalued intrinsic discount

Rising Genetic Testing And Precision Medicine Will Unlock New Markets

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1users have followed this narrative
AN
AnalystLowTarget
AnalystLowTarget·Updated
Fair Value US$70.00 77.3% undervalued intrinsic discount

Gene Therapy Infusion Delays And Safety Risks Will Spur Improvement

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0users have commented on this narrative
4users have followed this narrative
AN
AnalystConsensusTarget
AnalystConsensusTarget·Updated
Fair Value US$21.80 27.0% undervalued intrinsic discount

Upcoming ELEVIDYS And Gene Therapy Updates Will Restore Patient Trust

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1users have commented on this narrative
37users have followed this narrative

SRPT Community Fair Values

Recent SRPT News & Updates

No updates

Sarepta Therapeutics, Inc. Key Details

US$2.2b

Revenue

US$1.8b

Cost of Revenue

US$449.7m

Gross Profit

US$698.1m

Other Expenses

-US$248.4m

Earnings

Last Reported Earnings
Mar 31, 2025
Next Reporting Earnings
Aug 06, 2025
Earnings per share (EPS)
-2.53
Gross Margin
20.14%
Net Profit Margin
-11.12%
Debt/Equity Ratio
99.6%

Sarepta Therapeutics, Inc. Competitors

 
 
 
 
 
 
 
 
 
 
 
 

About SRPT

Founded
1980
Employees
1372
CEO
Douglas Ingram
WebsiteView website
www.sarepta.com

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 also developing SRP-9003, a limb-girdle muscular dystrophies gene therapy program. It has collaboration and license agreements with F. Hoffman-La Roche Ltd; Arrowhead Pharmaceuticals, Inc.; University of Western Australia; Catalent Maryland, Inc.; Nationwide Children’s Hospital; Dyno Therapeutics; Hansa Biopharma; Duke University; and Genethon. The company was incorporated in 1980 and is headquartered in Cambridge, Massachusetts.

U.S. Market Performance

  • 7 Days: -2.7%
  • 3 Months: 11.4%
  • 1 Year: 20.5%
  • Year to Date: 5.9%
Over the last 7 days, the market has dropped 2.7%, driven by a loss of 2.4% in the Information Technology sector. As for the longer term, the market has actually risen by 20% in the last year. Looking forward, earnings are forecast to grow by 15% annually. Market details ›
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