Compugen Ltd. (CGEN) Stock
Healthcare · Biotechnology · Member of Other US Stocks
Compugen Ltd. (CGEN) closed at USD 2.00 on 2026-10-14, a change of +17 % over the past year, with a market capitalization of USD 197.03M.
Compugen Ltd. recent closing prices
| Date | Close (USD) |
|---|---|
| 2026-10-14 | 2.00 |
| 2026-10-13 | 1.98 |
| 2026-10-12 | 2.07 |
| 2026-10-09 | 2.13 |
| 2026-10-08 | 2.12 |
| 2026-10-07 | 2.15 |
| 2026-10-06 | 2.22 |
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Compugen Ltd. key figures
- Previous close
- USD 2.00 (2026-10-14)
- 1-year change
- +17 %
- Market cap
- USD 197.03M
- Enterprise value
- USD 74.75M
- P/E ratio (trailing)
- 5.20
- P/E ratio (forward)
- -5.67
- EPS (trailing)
- 0.40
- EPS (forward)
- -0.37
- PEG ratio
- 1.29
- Price to book
- 2.22
- Revenue growth
- 107 %
- Earnings growth
- n/a
- Dividend per share (trailing)
- 0.00
- Short ratio
- 13.67
- Employees
- 75
- Analyst consensus (third-party)
- strong_buy
Source: Yahoo Finance via yfinance. Data may be delayed, incomplete or incorrect.
About Compugen Ltd.
Compugen Ltd., a clinical-stage therapeutic discovery and development company, engages in the research, development, and commercialization of therapeutics and product candidates in Israel, the United States, and Europe. The company's pipeline consists of COM701, an immuno-oncology pipeline program with an anti-PVRIG antibody; COM902, a therapeutic anti-TIGIT antibody, are in Phase 1 clinical trials and have been evaluated for the treatment of solid tumors as a monotherapy and in combination of PVRIG/PD-1 and PVRIG/TIGIT, as well as PVRIG/PD-1/TIGIT blockade; Bapotulimab, a therapeutic antibody targeting ILDR2 that is evaluated in Phase I clinical trials in patients with naïve head and neck squamous cell carcinoma; and Rilvegostomig, a novel anti- PD-1/TIGIT bispecific antibody, which is in Phase III clinical study in patients with advanced or metastatic non-small cell lung cancer. Its preclinical therapeutic pipeline also includes early-stage immuno-oncology programs focused to address various mechanisms of immune resistance; and COM503, high affinity antibody, which blocks the interaction between IL-18 binding protein and IL-18. The company has collaboration agreement with Bristol-Myers Squibb to evaluate the safety and tolerability of COM701 in combination with Bristol-Myers Squibb's PD-1 immune checkpoint inhibitor Opdivo in patients with advanced solid tumors. It has license agreement with AstraZeneca for the development of bi-specific and multi-specific immuno-oncology antibody products; and Gilead Sciences, Inc. for the research, development, manufacturing, and commercialization of COM503 and other products. The company was incorporated in 1993 and is headquartered in Holon, Israel.
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