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Sarepta Therapeutics

21.03

+0.17000.81%

Pre-market: 20.85-0.1800-0.86%08:18 EDT

Volume:2.66M

Turnover:55.56M

Market Cap:2.22B

PE:-15.98

High:21.16

Open:20.56

Low:20.18

Close:20.86

52wk High:25.32

52wk Low:14.68

Shares:105.57M

Float Shares:99.05M

Volume Ratio:0.78

T/O Rate:2.68%

Dividend:- -

Dividend Rate:- -

EPS(TTM):-1.3161

EPS(LYR):-7.1300

ROE:-9.48%

ROA:-1.13%

PB:1.45

PE(LYR):-2.95

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Overview Company News Filings

BUZZ-Sarepta rises after muscle disease drugs show promise in early-to-mid stage trials

Sarepta Therapeutics Inc - Proof-of-Concept Data Show Single Dose of Srp-1001 and Srp-1003 Reduces Target Protein or Mrna

THOMSON REUTERS

Sarepta Therapeutics Inc - Majority of Adverse Events in Studies Were Mild to Moderate and Not Dose Dependent

THOMSON REUTERS

Sarepta Therapeutics Inc - Sirna Achieves High Muscle Concentrations Without Dose Limiting Toxicity for Fshd1 and Dm1

THOMSON REUTERS

Analysts Conflicted on These Healthcare Names: Sarepta Therapeutics (SRPT), Rezolute (RZLT) and Demant (OtherWILLF)

Sarepta to present Phase 1/2 data for SRP-1001 in FSHD1 and SRP-1003 in DM1

Sarepta pre-May sNDA plan points to constructive FDA dialogue, says Oppenheimer

Sarepta provides regulatory update on Amondys 45, Vyondys 53

Sarepta plans FDA sNDA filings by end of April 2026 to seek traditional approval for AMONDYS 45 and VYONDYS 53

Sarepta Therapeutics Inc - FDA Confirms Sarepta Can Submit Essence Study and Real-World Evidence for Sndas

THOMSON REUTERS

Sarepta Provides Regulatory Update on Amondys 45® and Vyondys 53®

THOMSON REUTERS

Sarepta Therapeutics Inc - to Submit Sndas to FDA by End of April 2026 for Traditional Approval

THOMSON REUTERS

Sarepta Therapeutics Inc: Requested a Meeting With FDA to Discuss Submitting Supplemental New Drug Applications

THOMSON REUTERS

Cantor Fitzgerald Sticks to Its Hold Rating for Sarepta Therapeutics (SRPT)

Sarepta begins ENDEAVOR Cohort 8 trial of ELEVIDYS with sirolimus in 25 non-ambulant Duchenne patients

Analysts’ Top Healthcare Picks: Edgewise Therapeutics (EWTX), Sarepta Therapeutics (SRPT)

Sarepta Therapeutics Is Maintained at Outperform by Mizuho

Analysts Conflicted on These Healthcare Names: MoonLake Immunotherapeutics (MLTX), Sarepta Therapeutics (SRPT) and vTv Therapeutics (VTVT)

Sarepta Therapeutics Is Maintained at Sell by Citigroup

Sarepta price target raised to $9 from $8 at Citi

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The company’s...","market":"fut","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":{"source":"tipranks_highlight","url":"https://www.tipranks.com/news/blurbs/cantor-fitzgerald-sticks-to-its-hold-rating-for-sarepta-therapeutics-srpt-blurbs-news?utm_source=itigerup.com&utm_medium=referral","rn_cache_url":null,"directOrigin":true},"property":["rate"],"language":"en","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"https://www.tipranks.com/news/blurbs/cantor-fitzgerald-sticks-to-its-hold-rating-for-sarepta-therapeutics-srpt-blurbs-news?utm_source=itigerup.com&utm_medium=referral","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"0","news_top_title":null,"news_tag":"","news_rank":0,"length":0,"strategy_id":0,"source":"tipranks_highlight","symbols":["SRPT"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2619468254","title":"Sarepta begins ENDEAVOR Cohort 8 trial of ELEVIDYS with sirolimus in 25 non-ambulant Duchenne patients","url":"https://stock-news.laohu8.com/highlight/detail?id=2619468254","media":"Reuters","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2619468254?lang=en_us&edition=fundamental","pubTime":"2026-03-16 20:33","pubTimestamp":1773664423,"startTime":"0","endTime":"0","summary":"Sarepta reported that screening and enrollment have begun in Cohort 8 of the open-label Phase 1b ENDEAVOR study evaluating ELEVIDYS in non-ambulant males with Duchenne muscular dystrophy. The cohort plans to enroll about 25 U.S. participants who will receive prophylactic sirolimus starting 14 days before infusion and continuing for 12 weeks afterward. The regimen is intended to assess whether sirolimus can reduce acute liver injury risk associated with AAV gene therapy in non-ambulant patients. Primary endpoints include the incidence of acute liver injury and ELEVIDYS micro-dystrophin expression at 12 weeks. No study results were reported in the announcement.","market":"fut","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"en","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"https://api.refinitiv.com/data/news/v1/stories/urn:newsml:reuters.com:20260316:nNDL6zzcmT:1","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"0","news_top_title":null,"news_tag":"","news_rank":0,"length":0,"strategy_id":0,"source":null,"symbols":["IE00BFTCPJ56.SGD","IE0009355771.USD","IE00BJJMRZ35.SGD","SRPU","BK4585","SRPT","IE00B2B36J28.USD","IE0002141913.USD","IE00BJT1NW94.SGD","BK4139"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2619448180","title":"Analysts’ Top Healthcare Picks: Edgewise Therapeutics (EWTX), Sarepta Therapeutics 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