Sarepta Therapeutics, Inc.
Financials
Valuation Metrics
Sarepta Therapeutics, Inc.'s Market Cap is $2.12B. At end of 2025 it was $2.26B. Ranked #1960 of 3,121 in US market (top 63%), #744 of 1,463 on NASDAQ (top 51%), #129 of 266 in Pharmaceuticals, Biotechnology & Life Sciences (top 48%) by Market Cap.
Investment Metrics(as of 2026-09-18)
| Metric | Value | Rank |
|---|---|---|
| Size | ||
| Market Cap | $2.12B | US#1,960/3,121 Sec#129/266 |
| Revenue | $1.97B | US#1,445/3,121 Sec#39/266 |
| Net Income | $-137M | US—/3,121 Sec—/266 |
| Total Assets | $3.19B | US#1,772/3,121 Sec#45/266 |
| Net Assets | $1.53B | US#1,462/3,121 Sec#44/266 |
| Employees | 835 | US#2,068/3,121 Sec#60/266 |
| Value | ||
| P/B | 1.39x | US#812/3,121 Sec#32/266 |
| P/S | 1.08x | US#775/3,121 Sec#11/266 |
| FCF Yield | -6.19% | US—/3,121 Sec—/266 |
| Profitability | ||
| ROE | -8.95% | US#2,346/3,121 Sec#79/266 |
| ROA | -4.29% | US#2,494/3,121 Sec#85/266 |
| Op. Margin | -7.26% | US#2,519/3,121 Sec#92/266 |
| Revenue Growth | -20.44% | US#2,691/3,121 Sec#154/266 |
| Financial Health | ||
| Debt Ratio | 108.70% | US#1,182/3,121 Sec#171/266 |
| Total Debt | $1.05B | US#1,521/3,121 Sec#45/266 |
| FCF | $-131M | US#2,691/3,121 Sec#164/266 |
| Cash | $571M | US#980/3,121 Sec#50/266 |
| Current Ratio | 4.42x | US#539/3,121 Sec#161/266 |
| Performance | ||
| 1Y Return | 8.59% | US#1,125/3,121 Sec#154/266 |
| 1M Return | 1.93% | US#147/3,121 Sec#18/266 |
| From 52W High | -20.58% | US#1,381/3,121 Sec#96/266 |
| 1Y MDD | -39.22% | US#1,980/3,121 Sec#137/266 |
| Trading | ||
| Volume | 5,739,979 shares | US#694/3,121 Sec#67/266 |
| Trading Value | $116M | US#1,229/3,121 Sec#92/266 |
| Per Share | ||
| EPS | $-1.29 | US—/3,121 Sec—/266 |
| BPS | $14.47 | US#1,557/3,121 Sec#50/266 |
Company Info
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.