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Sarepta Therapeutics

18.79

-0.4300-2.24%

Post-market: 19.150.3600+1.92%19:34 EDT

Volume:1.67M

Turnover:31.88M

Market Cap:1.98B

PE:-14.28

High:19.73

Open:19.39

Low:18.66

Close:19.22

52wk High:25.32

52wk Low:14.68

Shares:105.57M

Float Shares:99.05M

Volume Ratio:0.66

T/O Rate:1.69%

Dividend:- -

Dividend Rate:- -

EPS(TTM):-1.3161

EPS(LYR):-7.1300

ROE:-9.48%

ROA:-1.13%

PB:1.30

PE(LYR):-2.64

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Overview Company News Filings

Morgan Stanley says Sarepta’s CEO transition brings clarity ahead of catalysts

Sarepta Gains After Appointing Former AbbVie Executive Severino as CEO

Sarepta Names Michael Severino CEO, Succeeding Retiring Doug Ingram

Sarepta Therapeutics - Doug Ingram to Retire and Serve as Advisor Until End of 2026

THOMSON REUTERS

Sarepta Therapeutics Appoints Michael Severino, M.d., Chief Executive Officer

THOMSON REUTERS

Press Release: Sarepta Therapeutics to Announce Second Quarter 2026 Financial Results

Analysts Offer Insights on Healthcare Companies: Compugen (CGEN), Telix Pharmaceuticals (OtherTLPPF) and Sarepta Therapeutics (SRPT)

Has Sarepta Therapeutics (SRPT) Fallen Below Fair Value After FDA Progress?

Simply Wall St.

Is Sarepta Therapeutics (SRPT) Undervalued Following FDA Progress On AMONDYS 45 And VYONDYS 53?

Simply Wall St.

Analysts Offer Insights on Healthcare Companies: Forte Biosciences (FBRX), Sarepta Therapeutics (SRPT) and Opus Genetics (IRD)

Sarepta Therapeutics Raised to Outperform from Peer Perform by Wolfe Research

Sarepta price target lowered to $20 from $23 at Piper Sandler

Sarepta upgraded to Outperform from Peer Perform at Wolfe Research

Why Sarepta Therapeutics (SRPT) Is Up 12.7% After FDA Accepts sNDAs Backed By ESSENCE Data

Simply Wall St.

H.C. Wainwright says Sarepta news does not signal full approvals

Sarepta Grants 151,305 Rsus to 30 New Hires Under 2024 Incentive Plan

Sarepta Therapeutics Announces Inducement Grants Under NASDAQ Listing Rule 5635(c)(4)

THOMSON REUTERS

Sarepta Shares up on FDA Acceptance of Supplemental New Drug Applications

Sarepta Therapeutics Gets FDA Review for Duchenne Muscular Dystrophy Applications

MT Newswires Live

Sarepta Says FDA Accepts Amondys 45, Vyondys 53 Sndas for Review, Sets Feb. 28, 2027 PDUFA Date

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on the shares. The firm lowers its Q2 El...","market":"fut","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":{"source":"tipranks_highlight","url":"https://www.tipranks.com/news/the-fly/sarepta-price-target-lowered-to-20-from-23-at-piper-sandler-thefly-news?utm_source=itigerup.com&utm_medium=referral","rn_cache_url":null,"directOrigin":true},"property":[],"language":"en","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"https://www.tipranks.com/news/the-fly/sarepta-price-target-lowered-to-20-from-23-at-piper-sandler-thefly-news?utm_source=itigerup.com&utm_medium=referral","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"-1","news_top_title":null,"news_tag":"","news_rank":0,"length":0,"strategy_id":0,"source":"tipranks_highlight","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":"2650991952","title":"Sarepta upgraded to Outperform from Peer Perform at Wolfe Research","url":"https://stock-news.laohu8.com/highlight/detail?id=2650991952","media":"TIPRANKS","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2650991952?lang=en_us&edition=fundamental","pubTime":"2026-07-09 05:10","pubTimestamp":1783545022,"startTime":"0","endTime":"0","summary":"Wolfe Research upgraded Sarepta (SRPT) to Outperform from Peer Perform with a $27 price target Share gains for Sarepta have been “transient” but th...","market":"fut","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":{"source":"tipranks_highlight","url":"https://www.tipranks.com/news/the-fly/sarepta-upgraded-to-outperform-from-peer-perform-at-wolfe-research-thefly-news?utm_source=itigerup.com&utm_medium=referral","rn_cache_url":null,"directOrigin":true},"property":[],"language":"en","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"https://www.tipranks.com/news/the-fly/sarepta-upgraded-to-outperform-from-peer-perform-at-wolfe-research-thefly-news?utm_source=itigerup.com&utm_medium=referral","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"1","news_top_title":null,"news_tag":"","news_rank":0,"length":0,"strategy_id":0,"source":"tipranks_highlight","symbols":["BK4139","IE00BFTCPJ56.SGD","IE00B2B36J28.USD","SRPU","SRPT","BK4585","IE0002141913.USD","IE00BJJMRZ35.SGD","IE00BJT1NW94.SGD","IE0009355771.USD"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2649907931","title":"Why Sarepta Therapeutics (SRPT) Is Up 12.7% After FDA Accepts sNDAs Backed By ESSENCE Data","url":"https://stock-news.laohu8.com/highlight/detail?id=2649907931","media":"Simply Wall St.","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2649907931?lang=en_us&edition=fundamental","pubTime":"2026-07-08 00:32","pubTimestamp":1783441923,"startTime":"0","endTime":"0","summary":"In late June 2026, Sarepta Therapeutics reported that the FDA accepted for filing supplemental New Drug Applications to convert accelerated approvals for its Duchenne muscular dystrophy therapies AMONDYS 45 and VYONDYS 53 into traditional approvals, supported by Phase 3 ESSENCE data and extensive real‑world evidence.\nAlthough the ESSENCE trial did not meet its primary endpoint, treatment-favoring trends, long-term safety data and real-world functional benefits could materially influence how...","market":"us","thumbnail":"https://images.simplywall.st/asset/industry/6111000-choice2-main-header/1585186599552","type":0,"news_type":0,"thumbnails":["https://images.simplywall.st/asset/industry/6111000-choice2-main-header/1585186599552"],"rights":{"source":"simplywall_highlight","url":"https://simplywall.st/stocks/us/pharmaceuticals-biotech/nasdaq-srpt/sarepta-therapeutics/news/why-sarepta-therapeutics-srpt-is-up-127-after-fda-accepts-sn","rn_cache_url":null,"directOrigin":true},"property":[],"language":"en","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"https://simplywall.st/stocks/us/pharmaceuticals-biotech/nasdaq-srpt/sarepta-therapeutics/news/why-sarepta-therapeutics-srpt-is-up-127-after-fda-accepts-sn","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"1","news_top_title":null,"news_tag":"productRelease","news_rank":0,"length":0,"strategy_id":0,"source":"simplywall_highlight","symbols":["BK4588","IE0009355771.USD","SRPU","BK4139","IE00BJT1NW94.SGD","SRPT","IE00BJJMRZ35.SGD","BK4585","IE00B2B36J28.USD","IE00BFTCPJ56.SGD","LABU","IE0002141913.USD"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2648514478","title":"H.C. Wainwright says Sarepta news does not signal full approvals","url":"https://stock-news.laohu8.com/highlight/detail?id=2648514478","media":"TIPRANKS","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2648514478?lang=en_us&edition=fundamental","pubTime":"2026-07-01 18:20","pubTimestamp":1782901236,"startTime":"0","endTime":"0","summary":"H.C. Wainwright analyst Mitchell Kapoor reiterates a Sell rating on Sarepta (SRPT) with a $5 price target after the FDA accepted the supplemental n...","market":"nz","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":{"source":"tipranks_highlight","url":"https://www.tipranks.com/news/the-fly/h-c-wainwright-says-sarepta-news-does-not-signal-full-approvals-thefly-news?utm_source=itigerup.com&utm_medium=referral","rn_cache_url":null,"directOrigin":true},"property":[],"language":"en","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"https://www.tipranks.com/news/the-fly/h-c-wainwright-says-sarepta-news-does-not-signal-full-approvals-thefly-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":["SRPU","IE0009355771.USD","IE0002141913.USD","IE00BJT1NW94.SGD","IE00BJJMRZ35.SGD","LABU","IE00B2B36J28.USD","IE00BFTCPJ56.SGD","BK4585","SRPT","BK4139","BK4588"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2648256416","title":"Sarepta Grants 151,305 Rsus to 30 New Hires Under 2024 Incentive Plan","url":"https://stock-news.laohu8.com/highlight/detail?id=2648256416","media":"Reuters","labels":["executive"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2648256416?lang=en_us&edition=fundamental","pubTime":"2026-07-01 04:25","pubTimestamp":1782851115,"startTime":"0","endTime":"0","summary":"Sarepta grants 151,305 RSUs to 30 new hires under 2024 incentive planSarepta Therapeutics granted 151,305 restricted stock units on June 30, 2026 to 30 second-quarter hires under its 2024 Employment C","market":"us","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:20260630:nNDL1G7nZ9:1","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"0","news_top_title":null,"news_tag":"executive","news_rank":0,"length":0,"strategy_id":0,"source":null,"symbols":["SRPT","IE00BJT1NW94.SGD","SRPU","IE0002141913.USD","IE0009355771.USD","IE00B2B36J28.USD","IE00BJJMRZ35.SGD","BK4139","BK4585","IE00BFTCPJ56.SGD"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2648902564","title":"Sarepta Therapeutics Announces Inducement Grants Under NASDAQ Listing Rule 5635(c)(4)","url":"https://stock-news.laohu8.com/highlight/detail?id=2648902564","media":"THOMSON REUTERS","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2648902564?lang=en_us&edition=fundamental","pubTime":"2026-07-01 04:25","pubTimestamp":1782851100,"startTime":"0","endTime":"0","summary":null,"market":"nz","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:20260630:nTUAGDQYV: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":"reuters_en_live","symbols":["IE0002141913.USD","IE00BFTCPJ56.SGD","BK4585","BK4139","SRPU","IE00BJT1NW94.SGD","IE00BJJMRZ35.SGD","SRPT","IE00B2B36J28.USD","IE0009355771.USD"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2648563682","title":"Sarepta Shares up on FDA Acceptance of Supplemental New Drug Applications","url":"https://stock-news.laohu8.com/highlight/detail?id=2648563682","media":"Dow Jones","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2648563682?lang=en_us&edition=fundamental","pubTime":"2026-07-01 00:38","pubTimestamp":1782837480,"startTime":"0","endTime":"0","summary":"Shares of Sarepta Therapeutics rose after the Food and Drug Administration accepted the company's supplemental new drug applications for two treatments for Duchenne muscular dystrophy.The stock gained 5.4% to $17.93 in midday trading on Tuesday. Shares are down 17% this year.Sarepta said the FDA has assigned a Prescription Drug User Fee Act target action data of Feb. 28, 2027 for the treatments, Amondys 45 and Vyondys 53.The submissions seek to convert the accelerated approvals of the drugs to traditional approvals, the company said.Analysts at Mizuho view the FDA filing acceptance as positive news, given investor concerns that the regulatory path forward could be limited after a Phase 3 trial evaluating the treatments failed to achieve statistical significance.\"We continue to believe the risk of Amondys 45/Vyondys 53 being withdrawn from the market remains low, given the clinical benefits demonstrated with real-world evidence and the ultra-rare nature of the exon 45 and exon 53 amenab","market":"other","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://dowjonesnews.com/newdjn/logon.aspx?AL=N","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"2","news_top_title":null,"news_tag":"productRelease","news_rank":0,"length":0,"strategy_id":0,"source":null,"symbols":["IE00BJJMRZ35.SGD","IE00BJT1NW94.SGD","LABU","BK4588","BK4585","IE00B2B36J28.USD","SRPU","BK4139","IE0009355771.USD","IE00BFTCPJ56.SGD","IE0002141913.USD","SRPT"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2647355905","title":"Sarepta Therapeutics Gets FDA Review for Duchenne Muscular Dystrophy Applications","url":"https://stock-news.laohu8.com/highlight/detail?id=2647355905","media":"MT Newswires Live","labels":["policyRegulatory"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2647355905?lang=en_us&edition=fundamental","pubTime":"2026-06-30 21:18","pubTimestamp":1782825508,"startTime":"0","endTime":"0","summary":"Sarepta Therapeutics  said Tuesday the US Food and Drug Administration has accepted its supplemental new drug applications for two treatments targeting Duchenne muscular dystrophy.The regulator established a target action date of Feb. 28, 2027, to complete its evaluation of both Amondys 45 and Vyondys 53, the company said.The company submitted the requests to transition the medical products from accelerated to standard approvals.Shares of the company rose more than 3% in Tuesday premarket activity.","market":"us","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://www.mtnewswires.com/","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"1","news_top_title":null,"news_tag":"policyRegulatory","news_rank":0,"length":0,"strategy_id":0,"source":"mtnewswires_news","symbols":["SRPU","IE00B2B36J28.USD","IE0009355771.USD","IE00BFTCPJ56.SGD","BK4585","IE0002141913.USD","IE00BJT1NW94.SGD","BK4588","IE00BJJMRZ35.SGD","BK4139","SRPT","LABU"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2647555730","title":"Sarepta Says FDA Accepts Amondys 45, Vyondys 53 Sndas for Review, Sets Feb. 28, 2027 PDUFA Date","url":"https://stock-news.laohu8.com/highlight/detail?id=2647555730","media":"Reuters","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2647555730?lang=en_us&edition=fundamental","pubTime":"2026-06-30 20:30","pubTimestamp":1782822645,"startTime":"0","endTime":"0","summary":"Sarepta says FDA accepts AMONDYS 45, VYONDYS 53 sNDAs for review, sets Feb. 28, 2027 PDUFA dateSarepta Therapeutics’ sNDAs for AMONDYS 45, VYONDYS 53 accepted by FDA for review to convert accelerated ","market":"us","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:20260630:nNDL51svWH:1","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"1","news_top_title":null,"news_tag":"productRelease","news_rank":0,"length":0,"strategy_id":0,"source":null,"symbols":["IE00B2B36J28.USD","SRPU","BK4585","SRPT","IE0002141913.USD","IE0009355771.USD","IE00BJT1NW94.SGD","IE00BFTCPJ56.SGD","IE00BJJMRZ35.SGD","BK4139"],"isVideo":false,"video":null,"gpt_icon":0}],"pageSize":20,"totalPage":9,"pageCount":2,"totalSize":171,"code":"91000000","status":"200"}]}}