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Compugen Ltd (CGEN)
NASDAQ:CGEN

Compugen (CGEN) AI Stock Analysis

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CGEN

Compugen

(NASDAQ:CGEN)

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Outperform 73 (OpenAI - 5.2)
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Outperform 73 (OpenAI - 5.2)
,
Outperform 73 (OpenAI - 5.2)
Rating:73Outperform
Price Target:
$2.50
▲(10.13% Upside)
Action:UpgradedDate:03/05/26
The score is driven primarily by the strengthened financial profile (profitability, cash generation, and low leverage) and supportive earnings-call outlook (extended runway and major partnerships). Offsetting this is the sustainability risk from deal-driven, partner-dependent revenue and only moderately strong technical momentum.
Positive Factors
Strong cash runway & low leverage
A $65M non-dilutive monetization plus ~$145.6M year‑end liquidity extends runway into 2029 and materially reduces near-term refinancing risk. Combined with very low reported leverage (debt-to-equity ~2.9%), this provides durable financial flexibility to fund clinical programs without immediate capital raises.
Validated strategic partnerships
Large collaborations with AstraZeneca and Gilead validate Compugen's discovery platform and provide substantial non-dilutive funding optionality and milestone upside. These partnerships broaden commercial pathways and risk‑share development, enabling pipeline advancement without sole reliance on internal capital.
High margins and positive cash conversion
Sharp 2025 inflection delivered high gross margins and strong net margins with operating and free cash flow converting near 99% of net income. Favorable unit economics and improved cash generation create durable capacity to fund R&D and reduce dilution pressure if milestone-driven revenues recur.
Negative Factors
Lumpy, partner-dependent revenue
The 2025 profitability and cash strength were largely driven by discrete upfronts and milestone receipts, not recurring product sales. This creates revenue volatility and forecasting difficulty over the 2–6 month horizon, making operating performance contingent on milestone timing rather than steady organic growth.
Clinical timeline risk for COM701
Delay of the COM701 MAIA interim readout to Q1 2027 lengthens the timeline for a critical clinical catalyst and milestone triggers. Extended timelines increase capital exposure, postpone potential partner payments, and raise event‑accumulation and enrollment risk that can affect near‑term value realization.
Limited control over partnered programs
Compugen depends on partners (AstraZeneca, Gilead) for development decisions and data disclosure, constraining its ability to time milestones or publicize results. This structural reliance reduces visibility into revenue realization and strategic optionality, and can delay recognition of value even when science or IP is promising.

Compugen (CGEN) vs. SPDR S&P 500 ETF (SPY)

Compugen Business Overview & Revenue Model

Company DescriptionCompugen Ltd., a clinical-stage therapeutic discovery and development company, researches, develops, and commercializes therapeutic and product candidates in Israel, the United States, and Europe. The company's immuno-oncology pipeline consists of COM701, an anti-PVRIG antibody that is in Phase I clinical study used for the treatment of solid tumors; COM902, a therapeutic antibody targeting TIGIT, which is in Phase I clinical study in patients with advanced malignancies as a monotherapy; Bapotulimab, a therapeutic antibody targeting ILDR2 that is in Phase I clinical study in patients with solid tumors; and AZD2936, a novel anti-TIGIT/PD-1 bispecific antibody, which is in Phase I/II clinical study in patients with advanced or metastatic non-small cell lung cancer. Its therapeutic pipeline also includes early-stage immuno-oncology programs focused primarily on myeloid targets. The company has collaboration agreement with Bayer Pharma AG for the research, development, and commercialization of antibody-based therapeutics against the company's immune checkpoint regulators; 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; and Johns Hopkins School of Medicine to evaluate novel T cell and myeloid checkpoint targets. It has license agreement with AstraZeneca for the development of bi-specific and multi-specific immuno-oncology antibody products; and research collaboration with Johns Hopkins University for myeloid. Compugen Ltd. was incorporated in 1993 and is headquartered in Holon, Israel.
How the Company Makes MoneyCompugen primarily makes money through (1) collaboration and licensing arrangements with larger pharmaceutical companies and (2) to a lesser extent, other operating income typical of early-stage biotech companies (e.g., grants or similar sources, if present in filings). Under collaboration/licensing deals, Compugen can earn upfront payments when a partnership is signed, research funding and cost reimbursements for work performed, development and regulatory milestone payments as partnered programs advance through clinical trials and approvals, and sales-based royalties if a partnered product reaches the market. In some agreements, Compugen may also be eligible for option fees (if a partner elects to take a license to a program after a defined research period) or co-development/cost-sharing economics depending on the structure of the deal. Because Compugen is clinical-stage, it generally does not rely on material product sales; instead, earnings are driven by the timing and success of partnered programs (which determine whether milestones and royalties are triggered) and by the recognition of collaboration revenue over time under applicable accounting rules. Specific active partnerships, product-level commercial revenue, and the exact mix of upfronts, milestones, and royalties are null if not available from the provided context.

Compugen Earnings Call Summary

Earnings Call Date:Mar 02, 2026
(Q4-2025)
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% Change Since: |
Next Earnings Date:May 18, 2026
Earnings Call Sentiment Positive
The call conveyed materially positive financial and operational developments: a meaningful non‑dilutive capital infusion ($65M) that extended the cash runway into 2029, a large year‑over‑year revenue and profitability swing driven by partner upfronts, validated partnerships with AstraZeneca and Gilead, and clinical progress for COM701 and GS‑0321 (trial initiations, conference presentations, and global site expansion). Offsetting these positives are risks and limitations: revenues are lumpy and dependent on partner milestones, a delay moved the COM701 interim analysis to Q1 2027 (though sites are now open), and program timing and data disclosure remain partly controlled by partners. Overall, highlights (cash runway, profitability, partnerships, clinical advancement) outweigh the lowlights (timing, revenue concentration, partner dependence), supporting a positive outlook but with continued execution and partner‑dependent milestones being key.
Q4-2025 Updates
Positive Updates
Extended Cash Runway and Strong Year‑End Cash Balance
Cash runway extended into 2029 (assuming no further cash inflows) via a non‑dilutive transaction with AstraZeneca. Year‑end cash, cash equivalents, short‑term deposits and marketable securities totaled approximately $145.6M, which includes the $65.0M upfront payment from AstraZeneca.
Substantial Revenue Increase Driven by Partner Upfronts
Reported revenue for quarter ended 12/31/2025 of ~$67.3M vs ~$1.5M in the comparable quarter of 2024 (~+4,387%), and revenue for the year ended 12/31/2025 of ~$72.8M vs ~$27.9M in 2024 (~+161%). 2025 revenues included the $65.0M AstraZeneca upfront and components of the Gilead upfront/IND milestone.
Swing to Profitability
Quarter ended 12/31/2025 net profit of ~$56.8M (~$0.60 per basic and diluted share) vs a net loss of ~$6.1M (~$0.07 per share loss) in the comparable quarter of 2024. Full‑year 2025 net profit of ~$35.3M (~$0.38 per share) vs a net loss of ~$14.2M (~$0.16 per share) in 2024—driven primarily by non‑recurring partner payments.
Clinical Advancement of COM701 (Ovarian Program)
Initiated dosing in the MAIA adaptive randomized maintenance trial of COM701 in platinum‑sensitive ovarian cancer and expanded trial footprint globally; 28 sites are now open across the U.S., Israel and France. Pooled Phase I data in platinum‑resistant ovarian cancer presented at ESMO showed COM701 was well tolerated with consistent durable responses in heavily pretreated patients, especially those without liver metastases, supporting exploration in earlier‑line maintenance settings.
Progress on GS‑0321 and Partner Funding
GS‑0321 (anti–IL‑18BP antibody) entered Phase I dose‑escalation/expansion (first patient dosed January 2025) and received scientific presentation at SITC. Gilead paid €60.0M upfront plus $30.0M on IND clearance; Compugen is eligible for up to an additional $758.0M in future milestones plus tiered royalties (single‑digit to low double‑digit).
Partnership Validation and Upside from Rilvegostomig
Strategic relationship with AstraZeneca validated by a monetization transaction and continued broad late‑stage development of rilvegostomig (AstraZeneca running ~10–11 active Phase III trials). Company retained majority of royalty interest and remains eligible for mid‑single‑digit tiered royalties; AstraZeneca previously estimated non‑risk‑adjusted peak annual revenue potential for rilvegostomig above $5.0B.
Controlled Operating Expenses
R&D expenses decreased to ~$5.5M for the quarter (vs ~$5.9M prior year quarter, approx. -6.8%) and ~$22.8M for the year (vs ~$24.8M prior year, approx. -8.1%). G&A expenses also declined modestly to ~$2.1M for the quarter (vs ~$2.2M, approx. -4.5%) and ~$8.9M for the year (vs ~$9.4M, approx. -5.3%), reflecting lower spend as prior trials wound down while selectively funding MAIA and early‑stage programs.
Negative Updates
Revenue Largely Lumpy and Deal‑Driven
2025 revenue growth was driven primarily by one‑time partner upfronts (AstraZeneca $65M upfront and Gilead payments). This produced a large, non‑recurring boost to profitability and cash, highlighting revenue concentration and ongoing dependence on partner milestones rather than recurring operating revenue.
Timing Delays in COM701 Interim Readout
Planned interim analysis for the MAIA COM701 trial moved from 2026 to Q1 2027 due to slower opening of major academic U.S. sites and slower event accumulation. Management noted sites are now fully open (28 sites) and the readout target is Q1 2027, but the shift underscores enrollment/timeline risks inherent to clinical development.
Dependence on Partners for Development and Data Disclosure
Progress and disclosure timelines for partnered programs are subject to partner control—AstraZeneca controls rilvegostomig decisions and data cadence; GS‑0321 data reporting must be coordinated with Gilead. This limits Compugen’s unilateral control over milestone timing and public data releases.
Clinical and Competitive Risk in TIGIT Field
Company acknowledged historical headwinds in the TIGIT field and emphasized differentiation by format and combination strategy, but success remains contingent on clinical outcomes from AstraZeneca’s broad rilvegostomig program and future COM902 development—introducing scientific and market risk.
Milestones and Future Payments Are Contingent
Remaining milestone economics for rilvegostomig total up to $195M (including a $25M BLA‑acceptance payment) and larger downstream milestones across partnerships (~up to ~$1.0B aggregate potential cited), but payments are contingent on clinical and regulatory events and thus uncertain in timing and probability.
Company Guidance
Management guided that, assuming no further cash inflows, Compugen’s cash runway now extends into 2029 supported by a 12/31/2025 cash balance of approximately $145.6 million (which included a $65.0 million upfront non‑dilutive payment from AstraZeneca); near‑term development milestones include an interim analysis for the COM701 MAIA ovarian trial in Q1 2027 and the next AstraZeneca trigger of BLA acceptance (an additional $25.0 million), which increases total remaining AZ milestones to up to $195.0 million (from $170.0 million); Gilead’s collaboration has already contributed €60.0 million upfront plus $30.0 million on IND clearance and leaves Compugen eligible for up to $758.0 million in further milestones plus single‑digit to low‑double‑digit royalties, and together the AstraZeneca and Gilead partnerships represent roughly up to $1.0 billion in potential milestones plus royalties (AstraZeneca has ~10 active Phase III rilvegostomig trials and previously estimated non‑risk‑adjusted peak annual revenue > $5.0 billion); financial guidance/metrics cited on the call included revenues of ~$67.3 million for Q4 2025 and ~$72.8 million for FY2025 (vs ~$1.5M and $27.9M in the comparable 2024 periods), R&D expense of ~$5.5M/Q4 and ~$22.8M FY2025 (vs $5.9M and $24.8M), G&A of ~$2.1M/Q4 and ~$8.9M FY2025 (vs $2.2M and $9.4M), and net profit of ~$56.8M (~$0.60 per share) for Q4 and ~$35.3M (~$0.38 per share) for FY2025 (vs net losses of ~$6.1M and ~$14.2M in 2024); management reiterated plans to use the runway to advance COM701 (28 sites open across the U.S., France and Israel), continue GS‑0321 (first patient dosed January 2025) and invest in the early‑stage pipeline.

Compugen Financial Statement Overview

Summary
Strong 2025 turnaround with sharply higher revenue, very high margins, and positive free cash flow alongside very low leverage. The key risk is durability: prior years showed operating losses and cash burn, and the 2025 step-change appears largely driven by lumpy partner payments.
Income Statement
74
Positive
Revenue and profitability inflected sharply in 2025, with revenue up ~1,240% year over year and strong profitability (net margin ~49%, EBIT margin ~43%). Gross margins have remained high across the period (~72%–97%), reflecting favorable unit economics. The main weakness is volatility: 2020–2024 showed persistent operating losses and negative net margins, with the 2025 step-change likely driven by lumpy collaboration/milestone-type revenue rather than a smooth operating trend.
Balance Sheet
82
Very Positive
Leverage is very low (debt-to-equity ~2.9% in 2025), which meaningfully reduces balance-sheet risk. Equity increased materially in 2025 and return on equity turned strongly positive (~34%) after several years of negative returns. The key watch item is variability in equity levels over time (notably lower in 2024 vs. prior years), underscoring that results and capital position can swing with profitability and financing dynamics.
Cash Flow
71
Positive
Cash generation improved meaningfully: operating cash flow and free cash flow were solidly positive in 2024 and 2025 (both years ~99% of net income converting to free cash flow, and operating cash flow running above net income). However, the cash-flow profile is uneven—2020–2023 showed sustained cash burn with negative operating and free cash flow—so durability of recent positive cash generation remains the primary risk.
BreakdownDec 2025Dec 2024Dec 2023Dec 2022Dec 2021
Income Statement
Total Revenue72.76M27.86M33.46M7.50M6.00M
Gross Profit63.51M19.93M31.45M6.53M5.32M
EBITDA31.80M-14.40M-12.52M-33.13M-34.61M
Net Income35.34M-14.23M-18.75M-33.69M-34.20M
Balance Sheet
Total Assets156.87M115.00M121.33M94.18M132.16M
Cash, Cash Equivalents and Short-Term Investments145.64M103.25M50.69M83.71M117.76M
Total Debt2.96M2.91M1.35M1.93M2.75M
Total Liabilities54.14M60.08M55.77M16.50M25.47M
Stockholders Equity102.73M54.91M65.56M77.68M106.69M
Cash Flow
Free Cash Flow31.33M49.49M-36.06M-34.99M-23.04M
Operating Cash Flow31.63M49.60M-35.89M-34.51M-22.75M
Investing Cash Flow30.00M-46.25M35.51M37.06M6.62M
Financing Cash Flow10.60M554.00K3.08M353.00K16.84M

Compugen Technical Analysis

Technical Analysis Sentiment
Positive
Last Price2.27
Price Trends
50DMA
1.91
Positive
100DMA
1.75
Positive
200DMA
1.67
Positive
Market Momentum
MACD
0.12
Negative
RSI
63.64
Neutral
STOCH
74.32
Neutral
Evaluating momentum and price trends is crucial in stock analysis to make informed investment decisions. For CGEN, the sentiment is Positive. The current price of 2.27 is above the 20-day moving average (MA) of 1.98, above the 50-day MA of 1.91, and above the 200-day MA of 1.67, indicating a bullish trend. The MACD of 0.12 indicates Negative momentum. The RSI at 63.64 is Neutral, neither overbought nor oversold. The STOCH value of 74.32 is Neutral, not indicating any strong overbought or oversold conditions. Overall, these indicators collectively point to a Positive sentiment for CGEN.

Compugen Risk Analysis

Compugen disclosed 79 risk factors in its most recent earnings report. Compugen reported the most risks in the "Tech & Innovation" category.
Finance & Corporate - Financial and accounting risks. Risks related to the execution of corporate activity and strategy
Latest Risks Added 0 New Risks

Compugen Peers Comparison

Overall Rating
UnderperformOutperform
Sector (51)
Financial Indicators
Name
Overall Rating
Market Cap
P/E Ratio
ROE
Dividend Yield
Revenue Growth
EPS Growth
73
Outperform
$214.64M4.0455.68%-88.47%-1658.33%
52
Neutral
$269.32M-1.51-53.83%-10.57%1.98%
52
Neutral
$230.74M-6.23-131.80%-16.26%
51
Neutral
$7.86B-0.30-43.30%2.27%22.53%-2.21%
50
Neutral
$425.81M-7.52-65.03%-84.46%33.32%
50
Neutral
$224.06M-3.95-5657.87%17.36%
47
Neutral
$164.79M-1.76-27.69%25.84%
* Healthcare Sector Average
Performance Comparison
Ticker
Company Name
Price
Change
% Change
CGEN
Compugen
2.27
0.70
44.59%
NKTX
Nkarta
2.32
0.79
51.63%
CCCC
C4 Therapeutics
2.76
0.68
32.69%
STTK
Shattuck Labs
5.95
4.79
412.93%
ELTX
Elicio Therapeutics
12.18
4.21
52.82%
NVCT
Nuvectis Pharma
8.71
-0.73
-7.73%

Compugen Corporate Events

Compugen Extends Cash Runway to 2029 and Swings to Profit on AstraZeneca Deal and Clinical Progress
Mar 2, 2026

Compugen on March 2, 2026, reported fourth-quarter and full-year 2025 results that showcased a dramatically strengthened balance sheet and extended cash runway into 2029, driven primarily by a $65 million non-dilutive royalty monetization deal with AstraZeneca for a small portion of rilvegostomig royalties. Revenues surged to $72.8 million in 2025 from $27.9 million a year earlier, turning a $14.2 million net loss in 2024 into a $35.3 million net profit in 2025, while the company maintained zero debt and trimmed R&D and G&A expenses.

Operationally, Compugen advanced its clinical portfolio in 2025 by initiating dosing in the MAIA-ovarian maintenance trial of COM701 and a Phase 1 trial of GS-0321 with partner Gilead, expanding its trial footprint across the U.S., Israel and France, and presenting new data for COM701 and GS-0321 at major oncology meetings. The company also highlighted AstraZeneca’s promising Phase 2 data and 10 ongoing Phase 3 trials for rilvegostomig, leadership changes including the appointment of Dr. Eran Ophir as president and CEO and the transition of Dr. Anat Cohen-Dayag to executive chair, and confirmed it remains on track for an interim MAIA-ovarian analysis in the first quarter of 2027, reinforcing its positioning as a well-funded, AI-driven immuno-oncology innovator with de-risking partnerships.

The most recent analyst rating on (CGEN) stock is a Buy with a $2.00 price target. To see the full list of analyst forecasts on Compugen stock, see the CGEN Stock Forecast page.

Compugen Adds Veteran Healthcare Strategist Michele Holcomb to Board of Directors
Feb 12, 2026

On February 11, 2026, Compugen appointed healthcare strategist Michele Holcomb, Ph.D., as an independent director to its board, a move disclosed in a February 12, 2026 filing and press release. Her term will run until after the 2026 annual general meeting, reinforcing the company’s governance as it advances multiple clinical programs and navigates key value-creation milestones.

Holcomb brings more than 30 years of experience across biotech, pharmaceuticals and healthcare services, including senior roles at Cardinal Health, Teva and McKinsey. Her background in strategy, business development and complex partnerships is expected to bolster Compugen’s ability to leverage its AI-driven discovery engine, manage its pipeline and collaborations, and support long-term value for patients and shareholders.

The most recent analyst rating on (CGEN) stock is a Buy with a $2.00 price target. To see the full list of analyst forecasts on Compugen stock, see the CGEN Stock Forecast page.

Glossary
BuyA stock rated as a "Buy" is expected to perform better than the overall market or a specific benchmark over the near-to-medium term. This rating suggests the stock is likely to deliver higher returns compared to other stocks in the same sector or market index. Note: This is not investment advice; please consult a financial advisor before making investment decisions.
HoldA stock rated as a "Hold" is expected to perform in line with the overall market or a specific benchmark. This rating indicates that the stock is neither particularly compelling nor unfavorable for investment. Note: This is not investment advice; please consult a financial advisor before making investment decisions.
SellA stock rated as a "Sell" is expected to perform worse than the overall market or a specific benchmark over the near-to-medium term. This rating suggests the stock may deliver lower returns compared to other stocks in the same sector or market index. Note: This is not investment advice; please consult a financial advisor before making investment decisions.

Disclaimer

This AI Analyst Stock Report is automatically generated by our AI systems using advanced algorithms and publicly available financial, technical, and market data. While the information provided aims to be accurate and insightful, it is intended for informational purposes only and should not be considered financial advice. Any content created by an AI (Artificial Intelligence) system may contain inaccuracies and/or contain errors. Investing in stocks carries inherent risks, and past performance is not indicative of future results. This report does not account for your personal financial circumstances, objectives, or risk tolerance. Always conduct your own research or consult with a qualified financial advisor before making investment decisions. The analysis and recommendations provided are based on historical and current data and may not fully reflect future market conditions or unexpected developments. Neither the creators of this report nor its affiliated entities guarantee the accuracy, completeness, or reliability of the information presented. Use this report at your own discretion and risk.Date of analysis: Mar 05, 2026