MARKET

SRPT

SRPT

Sarepta Therapeutics Inc
NASDAQ
118.65
+1.53
+1.31%
Opening 13:13 04/24 EDT
OPEN
117.66
PREV CLOSE
117.12
HIGH
118.81
LOW
117.21
VOLUME
284.79K
TURNOVER
0
52 WEEK HIGH
159.89
52 WEEK LOW
55.25
MARKET CAP
11.14B
P/E (TTM)
-20.4544
1D
5D
1M
3M
1Y
5Y
Press Release: Sarepta Therapeutics to Announce First Quarter 2024 Financial Results
Sarepta Therapeutics to announce first quarter 2024 financial results after the Nasdaq Global Market closes on May 1, 2024. The Company is the leader in precision genetic medicine for rare diseases. The company will host a conference call to discuss its financial results. The event will be webcast live on Sarepta's website.
Dow Jones · 9h ago
SAREPTA THERAPEUTICS TO ANNOUNCE FIRST QUARTER 2024 FINANCIAL RESULTS
Reuters · 9h ago
GSK Gears Up for Q1 Earnings: Here's What to Expect
NASDAQ · 1d ago
Edgewise gets EU orphan drug status for muscular dystrophy drug
Edgewise gets EU orphan drug status for muscular dystrophy drug. Edgewise Therapeutics has received orphan drug designation from EU regulators for its drug candidate sevasemten. The drug candidate is in the treatment of Becker muscular dy Strophy and Duchenne muscular dystrophy.
Seeking Alpha · 1d ago
AbbVie (ABBV) to Report Q1 Earnings: What's in the Cards?
NASDAQ · 2d ago
Henry Schein (HSIC) Gears Up for Q1 Earnings: Factors to Note
NASDAQ · 2d ago
Weekly Report: what happened at SRPT last week (0415-0419)?
Weekly Report · 2d ago
Viking (VKTX) to Report Q1 Earnings: What's in the Cards?
NASDAQ · 5d ago
More
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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