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Sarepta Therapeutics Inc

Gesloten

SectorGezondheidszorg

15.69 -1.2

Overzicht

Wijziging aandelenprijs

24u

Huidig

Min

15.63

Max

15.92

Belangrijke statistieken

By Trading Economics

Inkomsten

614M

331M

Verkoop

288M

731M

K/W

Sectorgemiddelde

48.086

62.58

EPS

3.16

Winstmarge

45.287

Werknemers

835

EBITDA

628M

375M

Aanbevelingen

By TipRanks

Aanbevelingen

Neutraal

12 Maanden Prognose

+46.24% upside

Dividenden

By Acuity

Volgende Winsten

5 aug 2026

Marktinformatie

By TradingEconomics

Marktkapitalisatie

-550M

1.8B

Vorige openingsprijs

16.89

Vorige sluitingsprijs

15.69

Nieuwssentiment

By Acuity

80%

20%

310 / 340 Rangschikking in Healthcare

Sarepta Therapeutics Inc Grafiek

Eerdere prestaties zijn geen betrouwbare indicator voor toekomstige resultaten.

Gerelateerd nieuws

21 jul 2026, 17:51 UTC

Sarepta Therapeutics shares are lower today, pulling back from earlier session highs amid no specific news. The stock remains near the lower end of its one-month range.

Peer Vergelijking

Prijswijziging

Sarepta Therapeutics Inc Prognose

Koersdoel

By TipRanks

46.24% opwaarts potentieel

12 Maanden Prognose

Gemiddelde 22.93 USD  46.24%

Hoogste 38 USD

Laagste 5 USD

Gebaseerd op 16 Wall Street-analisten die 12-maands prijsdoelen bieden voor Sarepta Therapeutics Inc - Dist. in de afgelopen 3 maanden.

Beoordelingsconsensus

By TipRanks

Neutraal

16 ratings

5

Buy

7

Hold

4

Sell

Sentiment

By Acuity

310 / 340 Rangschikking in Gezondheidszorg

Nieuwssentiment

Zeer Sterk Bearish Bewijs

Volatiliteit

Onder gemiddelde

Nieuws Volume (RCV)

Gemiddelde

Financieel

Verkoop- en administratiekosten

Bedrijfskosten

Winst voor belastingen

Verkoop

Kosten van verkopen

Brutowinst op verkopen

Rente-uitgaven op schulden

EBITDA

Operationele winst

$

Over Sarepta Therapeutics Inc

Sarepta Therapeutics, Inc., a commercial-stage biopharmaceutical company, focuses on the discovery and development of RNA-targeted therapeutics, gene therapies, and other genetic therapeutic modalities for the treatment of rare diseases. It offers EXONDYS 51 injection to treat duchenne muscular dystrophy (duchenne) in patients with confirmed mutation of the dystrophin gene that is amenable to exon 51 skipping; VYONDYS 53 for the treatment of duchenne in patients with confirmed mutation of the dystrophin gene that is amenable to exon 53 skipping; AMONDYS 45 for the treatment of duchenne in patients with confirmed mutation of the dystrophin gene; and ELEVIDYS, an adeno-associated virus based gene therapy for the treatment of ambulatory pediatric patients aged 4 through 5 years with duchenne with a confirmed mutation in the duchenne gene. The company is also developing SRP-5051, a peptide conjugated PMO that binds exon 51 of dystrophin pre-mRNA; and SRP-9003, a limb-girdle muscular dystrophies gene therapy program. It has collaboration and license agreements with F. Hoffman-La Roche Ltd; Nationwide Children's Hospital; Genevant Sciences; University of Florida; Dyno Therapeutics; Hansa Biopharma; Duke University; Genethon; and StrideBio. The company was incorporated in 1980 and is headquartered in Cambridge, Massachusetts.
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