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Sarepta Therapeutics, Inc.

SRPT· NASDAQ
$15.88+6.86%
2026-08-03

Financials

Valuation Metrics

Sarepta Therapeutics, Inc.'s Market Cap is $1.68B. At end of 2025 it was $2.26B. Ranked #2181 of 3,112 in US market (top 70%), #857 of 1,445 on NASDAQ (top 59%), #155 of 269 in Pharmaceuticals, Biotechnology & Life Sciences (top 58%) by Market Cap.

Investment Metrics(as of 2026-08-03)

MetricValue
Size
Market Cap$1.68B
Revenue$2.18B
Net Income$65M
Total Assets$3.18B
Net Assets$1.51B
Employees835
Value
P/E25.77x
P/B1.11x
P/S0.77x
EV/EBITDA18.00x
FCF Yield6.33%
Profitability
ROE4.32%
ROA2.05%
Op. Margin-1.88%
Revenue Growth-1.89%
Earnings Growth-403.27%
Financial Health
Debt Ratio111.21%
Total Debt$1.04B
FCF$106M
Cash$464M
Current Ratio4.63x
Net Debt/EBITDA4.58x
Performance
1Y Return-0.19%
1M Return-17.63%
From 52W High-37.28%
1Y MDD-63.10%
Trading
Volume3,360,075 shares
Trading Value$52M
Per Share
EPS$-6.81
BPS$10.88

Company Info

CEO Mr. Douglas S. Ingram Esq., J.D.
Employees 835
HQ Cambridge, United States

Sarepta Therapeutics, Inc., a commercial-stage biopharmaceutical company, focuses on the discovery and development of RNA-targeted therapeutics, siRNA platform, gene therapy, and other genetic therapeutic modalities for the treatment of rare diseases. It offers EXONDYS 51 for the treatment of Duchenne in patients who have a confirmed mutation of the dystrophin gene that is amenable to exon 51 skipping; VYONDYS 53 for the treatment of Duchenne in patients who have a confirmed mutation of the dystrophin gene that is amenable to exon 53 skipping; AMONDYS 45 for the treatment of Duchenne in patients who have a confirmed mutation of the dystrophin gene that is amenable to exon 45 skipping; and ELEVIDYS, an AAV-based gene therapy, which is contraindicated in patients with any deletion in exon 8 and/or exon 9 in the Duchenne gene. The company also develops SRP-9003, a gene therapy program for the treatment of LGMD2E; SRP-1001 to selectively target and knockdown DUX4 using RNAi in Phase 1/2a clinical trials; and SRP-1003 for reduction of expression of the DMPK gene in Phase 1/2a clinical trials. It has collaboration and license agreements with F. Hoffman-La Roche Ltd; Arrowhead Pharmaceuticals, Inc.; University of Western Australia; Nationwide Children's Hospital; Hansa Biopharma; and Duke University. The company was incorporated in 1980 and is headquartered in Cambridge, Massachusetts.