Sarepta Therapeutics, Inc. (SRPT) Stock
Healthcare · Biotechnology · Member of Other US Stocks
Sarepta Therapeutics, Inc. (SRPT) closed at USD 16.83 on 2026-10-14, a change of -30.5 % over the past year, with a market capitalization of USD 1.88B.
Sarepta Therapeutics, Inc. recent closing prices
| Date | Close (USD) |
|---|---|
| 2026-10-14 | 16.83 |
| 2026-10-13 | 16.51 |
| 2026-10-12 | 17.44 |
| 2026-10-09 | 17.85 |
| 2026-10-08 | 18.21 |
| 2026-10-07 | 17.50 |
| 2026-10-06 | 17.31 |
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Sarepta Therapeutics, Inc. key figures
- Previous close
- USD 16.83 (2026-10-14)
- 1-year change
- -30.5 %
- Market cap
- USD 1.88B
- Enterprise value
- USD 2.15B
- P/E ratio (trailing)
- -11.33
- P/E ratio (forward)
- 7.38
- EPS (trailing)
- -1.57
- EPS (forward)
- 2.41
- PEG ratio
- -0.09
- Price to book
- 1.23
- Revenue growth
- -34.3 %
- Earnings growth
- n/a
- Dividend per share (trailing)
- 0.00
- Short ratio
- 7.77
- Employees
- 835
- Analyst consensus (third-party)
- hold
Source: Yahoo Finance via yfinance. Data may be delayed, incomplete or incorrect.
About Sarepta Therapeutics, Inc.
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.
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