Sarepta Therapeutics, Inc.
Financials
Valuation Metrics
Sarepta Therapeutics, Inc.'s Market Cap is $1.93B. At end of 2025 it was $2.26B. Ranked #1978 of 3,116 in US market (top 63%), #744 of 1,472 on NASDAQ (top 51%), #138 of 265 in Pharmaceuticals, Biotechnology & Life Sciences (top 52%) by Market Cap.
Investment Metrics(as of 2026-11-02)
| Metric | Value | Rank |
|---|---|---|
| Size | ||
| Market Cap | $1.93B | US#1,978/3,116 Sec#138/265 |
| Revenue | $1.97B | US#1,427/3,116 Sec#39/265 |
| Net Income | $-137M | US—/3,116 Sec—/265 |
| Total Assets | $3.19B | US#1,763/3,116 Sec#45/265 |
| Net Assets | $1.53B | US#1,454/3,116 Sec#44/265 |
| Employees | 835 | US#2,058/3,116 Sec#60/265 |
| Value | ||
| P/B | 1.27x | US#732/3,116 Sec#32/265 |
| P/S | 0.98x | US#725/3,116 Sec#11/265 |
| FCF Yield | -6.80% | US—/3,116 Sec—/265 |
| Profitability | ||
| ROE | -8.95% | US#2,337/3,116 Sec#79/265 |
| ROA | -4.29% | US#2,491/3,116 Sec#86/265 |
| Op. Margin | -7.26% | US#2,489/3,116 Sec#91/265 |
| Revenue Growth | -20.44% | US#2,642/3,116 Sec#150/265 |
| Financial Health | ||
| Debt Ratio | 108.70% | US#1,173/3,116 Sec#168/265 |
| Total Debt | $1.05B | US#1,500/3,116 Sec#45/265 |
| FCF | $-131M | US#2,692/3,116 Sec#166/265 |
| Cash | $571M | US#982/3,116 Sec#51/265 |
| Current Ratio | 4.42x | US#528/3,116 Sec#158/265 |
| Performance | ||
| 1Y Return | -23.72% | US#2,365/3,116 Sec#190/265 |
| 1M Return | 4.66% | US#1,502/3,116 Sec#96/265 |
| From 52W High | -25.79% | US#1,641/3,116 Sec#96/265 |
| 1Y MDD | -37.64% | US#1,904/3,116 Sec#119/265 |
| Trading | ||
| Volume | 881,094 shares | US#1,403/3,116 Sec#139/265 |
| Trading Value | $16M | US#1,861/3,116 Sec#143/265 |
| Per Share | ||
| EPS | $-1.29 | US—/3,116 Sec—/265 |
| BPS | $14.47 | US#1,549/3,116 Sec#49/265 |
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.