| Breakdown | TTM | Dec 2024 | Dec 2023 | Dec 2022 | Dec 2021 | Dec 2020 |
|---|---|---|---|---|---|---|
Income Statement | ||||||
| Total Revenue | 7.50M | 27.86M | 33.46M | 7.50M | 6.00M | 2.00M |
| Gross Profit | 6.53M | 19.93M | 31.45M | 6.53M | 5.32M | 1.94M |
| EBITDA | -34.01M | -14.40M | -12.52M | -33.13M | -34.61M | -28.94M |
| Net Income | -31.56M | -14.23M | -18.75M | -33.69M | -34.20M | -29.70M |
Balance Sheet | ||||||
| Total Assets | 67.61M | 115.00M | 121.33M | 94.18M | 132.16M | 138.32M |
| Cash, Cash Equivalents and Short-Term Investments | 57.51M | 103.25M | 50.69M | 83.71M | 117.76M | 124.43M |
| Total Debt | 1.41M | 2.91M | 1.35M | 1.93M | 2.75M | 3.17M |
| Total Liabilities | 14.38M | 60.08M | 55.77M | 16.50M | 25.47M | 18.53M |
| Stockholders Equity | 53.23M | 54.91M | 65.56M | 77.68M | 106.69M | 119.78M |
Cash Flow | ||||||
| Free Cash Flow | -23.38M | 49.49M | -36.06M | -34.99M | -23.04M | -28.49M |
| Operating Cash Flow | -23.03M | 49.60M | -35.89M | -34.51M | -22.75M | -28.32M |
| Investing Cash Flow | 40.39M | -46.25M | 35.51M | 37.06M | 6.62M | -82.17M |
| Financing Cash Flow | -18.41M | 554.00K | 3.08M | 353.00K | 16.84M | 108.46M |
Name | Overall Rating | Market Cap | P/E Ratio | ROE | Dividend Yield | Revenue Growth | EPS Growth |
|---|---|---|---|---|---|---|---|
56 Neutral | $164.62M | ― | -35.66% | ― | -48.16% | -97.37% | |
51 Neutral | $7.86B | -0.30 | -43.30% | 2.27% | 22.53% | -2.21% | |
48 Neutral | $153.25M | ― | -150.12% | ― | ― | 10.63% | |
47 Neutral | $228.94M | ― | -52.99% | ― | 16.55% | 16.73% | |
43 Neutral | $114.30M | ― | -73.39% | ― | -27.33% | 34.66% | |
39 Underperform | $169.75M | ― | -26.94% | ― | ― | 26.33% | |
30 Underperform | $152.76M | ― | -9999.00% | ― | ― | -4.60% |
On October 13, 2025, Compugen Ltd. announced the presentation of a pooled analysis of COM701 in three Phase 1 trials for patients with platinum-resistant ovarian cancer at the ESMO 2025 conference. The analysis, which included 60 evaluable patients, demonstrated that COM701 was well tolerated and showed durable responses, particularly in patients without liver metastases. This supports the rationale for its use as maintenance therapy in earlier treatment settings. Compugen is currently conducting the MAIA-ovarian trial to assess COM701 as a maintenance treatment in relapsed platinum-sensitive ovarian cancer, with interim analysis results expected by the end of 2026. The company is expanding trial sites to include locations in the U.S., Israel, and France, and anticipates its cash reserves will support operations into 2027.
On September 16, 2025, Compugen Ltd. conducted its 2025 Annual General Meeting of Shareholders, where all proposals were approved by the necessary majority vote. This approval signifies continued shareholder support and could potentially strengthen Compugen’s strategic initiatives and market position in the biotechnology sector.
On August 6, 2025, Compugen Ltd. announced the distribution of its proxy statement to shareholders for the upcoming annual general meeting scheduled for September 16, 2025, in Israel. The meeting will address the election of seven directors, approval of compensation for incoming executives, and re-appointment of the company’s independent accounting firm. This event is significant for stakeholders as it involves key decisions on leadership and financial oversight, impacting the company’s strategic direction and governance.
Compugen Ltd. reported its second quarter 2025 financial results on August 6, 2025, highlighting significant advancements in its immuno-oncology pipeline. The company dosed the first patient in its MAIA-ovarian trial for COM701 and is preparing to present a pooled analysis of Phase 1 trials at ESMO 2025. Compugen’s partner, AstraZeneca, is progressing with its rilvegostomig program, which could become a significant revenue source for Compugen. Financially, the company maintains a solid position with a cash runway expected to fund operations into 2027, despite a decrease in revenue compared to the previous year.