MARKET

SRPT

SRPT

Sarepta Therapeutics Inc
NASDAQ
143.90
-3.66
-2.48%
Opening 15:32 07/26 EDT
OPEN
147.94
PREV CLOSE
147.56
HIGH
148.12
LOW
143.31
VOLUME
368.96K
TURNOVER
0
52 WEEK HIGH
173.25
52 WEEK LOW
55.25
MARKET CAP
13.60B
P/E (TTM)
1805.52
1D
5D
1M
3M
1Y
5Y
1D
Sarepta Therapeutics' Pullback After Recent FDA Approval A Buying Opportunity
Seeking Alpha · 2d ago
Oppenheimer Sticks to Their Buy Rating for Sarepta Therapeutics (SRPT)
TipRanks · 2d ago
Weekly Report: what happened at SRPT last week (0715-0719)?
Weekly Report · 4d ago
Notable ETF Outflow Detected - XBI, EXAS, SRPT, UTHR
NASDAQ · 07/19 14:58
Here's How Much $1000 Invested In Sarepta Therapeutics 10 Years Ago Would Be Worth Today
Sarepta Therapeutics has outperformed the market over the past 10 years by 10.36% on an annualized basis. The company has an average annual return of 21.14%. If an investor bought $1000 of SRPT stock 10 years ago, it would be worth $6,642.60 today.
Benzinga · 07/18 18:30
Buy Rating Affirmed for Sarepta Therapeutics Amid Strong Elevidys Demand and Strategic Growth Outlook
TipRanks · 07/18 07:18
SAVA Stock Plunges as Cassava Sciences CEO Steps Down. What to Know.
Investorplace · 07/17 16:11
Jim Cramer Says Don't Sell Match Group: 'You've Just Got A Very, Very Smart Investor In There'
Jim Cramer said Fortinet, Inc. Is not his favorite stock. He said Air Products and Chemicals is a better run company than Linde plc. Cramer recommended not selling Match Group, Inc (NASDAQ:MTCH) The "Mad Money" host said Costco is the best of the breed.
Benzinga · 07/17 12:55
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About SRPT
Sarepta Therapeutics, Inc. is a commercial-stage biopharmaceutical company. The Company is focused on helping patients through the discovery and development of ribonucleic acid (RNA)-targeted therapeutics, gene therapy and other genetic therapeutic modalities for the treatment of rare diseases. It has developed multiple approved products for the treatment of Duchenne muscular dystrophy (Duchenne) and is developing potential therapeutic candidates for a range of diseases and disorders, including Duchenne, Limb-girdle muscular dystrophies (LGMDs) and other neuromuscular and central nervous system (CNS) related disorders. It has developed and commercialized four approved products for the treatment of Duchenne: EXONDYS 51 (eteplirsen), Injection (EXONDYS 51), VYONDYS 53 (golodirsen) Injection (VYONDYS 53), AMONDYS 45 (casimersen) Injection (AMONDYS 45), and ELEVIDYS. Its pipeline includes approximately 40 programs at various stages of discovery, pre-clinical and clinical development.

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