SRPT Sarepta Therapeutics, Inc. logo

SRPT Sarepta Therapeutics, Inc.

Healthcare
$16.80-0.94%ClosedMarket Cap: $1.77B

As of 2026-05-25

Valuation

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P/E (TTM)

PEG

P/B

1.17

P/S

0.81

EV/EBITDA

18.77

DCF Value

$-1,274.69

FCF Yield

6.0%

Div Yield

0.0%

Margins & Returns

Gross Margin

62.4%

Operating Margin

-1.9%

Net Margin

3.0%

ROE

4.9%

ROA

2.0%

ROIC

-1.5%

Financials

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PeriodRevenueNet IncomeEPS
Q1 null$730.8M$331.0M$
Q4 null$442.9M$-282.8M$
FY null$2.20B$-713.4M$
Q3 null$399.4M$-179.9M$

Analyst Ratings

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Consensus

Hold

Target (Consensus)

$25.14

Target (Median)

$25.00

Target Range

$14.00 - $35.00

0 Strong Buy8 Buy13 Hold3 Sell2 Strong Sell
HC Wainwright & Co.Sell
2026-04-16
NeedhamUnderperform
2026-03-26
CitigroupSell
2026-03-26
OppenheimerOutperform
2026-03-19
MizuhoOutperform
2026-03-13

Trading Activity

Insider Trades

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Wong Ryan Ho-Yanofficer: Chief Financial Officer
SellFri Mar 13
Rothfuss Cristinofficer: EVP, General Counsel
SellFri Mar 13
Rodino-Klapac Louiseofficer: President, R&D and Tech Ops
SellFri Mar 13
Mayo Stephendirector
SellFri Mar 13
Estepan Ian Michaelofficer: Chief Operating Officer
SellFri Mar 13

Company Info

Sector

Healthcare

Industry

Biotechnology

Country

US

Exchange

Beta

0.26

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; and VYONDYS 53 for the treatment of duchenne in patients with confirmed mutation of the dystrophin gene that is amenable to exon 53 skipping. The company is also developing AMONDYS 45, a product candidate that uses phosphorodiamidate morpholino oligomer chemistry and exon-skipping technology to skip exon 45 of the dystrophin gene; SRP-5051, a peptide conjugated PMO that binds exon 51 of dystrophin pre-mRNA; SRP-9001, a DMD micro-dystrophin gene therapy program; and SRP-9003, a limb-girdle muscular dystrophies gene therapy program. It has collaboration agreements with F. Hoffman-La Roche Ltd; Nationwide Children's Hospital; Lysogene; Duke University; Genethon; and StrideBio. The company was incorporated in 1980 and is headquartered in Cambridge, Massachusetts.

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