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Sarepta Therapeutics

20.48

+0.51002.55%

Post-market: 20.650.1700+0.83%19:55 EDT

Volume:2.92M

Turnover:59.42M

Market Cap:2.15B

PE:-2.87

High:20.62

Open:19.93

Low:19.81

Close:19.97

52wk High:72.05

52wk Low:10.42

Shares:104.79M

Float Shares:95.17M

Volume Ratio:0.43

T/O Rate:3.07%

Dividend:- -

Dividend Rate:- -

EPS(TTM):-7.1300

EPS(LYR):-7.1300

ROE:-53.47%

ROA:-11.24%

PB:1.88

PE(LYR):-2.87

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Overview Company News Filings

Shares of This Gene Therapy Maker Are Up 29%. The Safety Debate Is Far From Over. -- Barrons.com

Sarepta initial siRNA data ‘thin and somewhat mixed,’ says Leerink

Sarepta early DM1 data ‘appear promising,’ says Oppenheimer

Sarepta Therapeutics' Early Trial Results of siRNA Treatments Show High Muscle Concentrations in Neuromuscular Diseases

MT Newswires Live

Shares of Sarepta Therapeutics up 3.2% Premarket After Muscle Disease Drugs Show Promise in Early-to-Mid Stage Trials

THOMSON REUTERS

BRIEF-Sarepta Announces First Clinical Data From Sirna Pipeline Targeting Fshd1 And Dm1

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)

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The stock spiked 29% to $22.67 on Wednesday, on pace for the largest single-day percent increase since June 2024, according to Dow Jones Market Data. The benchmark S&P 500 ticked up 0.6%.But investors may have been getting ahead of themselves. 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