CGENNasdaqBiological Products, (No Diagnostic Substances)US GAAP · USD

Compugen Ltd

Compugen Ltd. is a U.S.-listed, Israel-based biopharmaceutical company focused on computationally discovered cancer immunotherapy programs. The company develops antibody-based drug candidates and also licenses selected programs to larger pharmaceutical partners for further development and commercialization.

Revenue72.8m USD
+161.1 %y/y
Operating profit (EBIT)31.3m USD
+310.4 %y/y
EBIT margin43.1%
+96.5 ppy/y
Net income35.3m USD
+348.4 %y/y
Free cash flow31.3m USD
−36.7 %y/y

Fiscal year 2025 · change from previous year

Development 2020–2025

-50-250255075m USD2020: 2.0 m USD2020: EBIT -31 m USD20202021: 6.0 m USD2021: EBIT -35 m USD20212022: 7.5 m USD2022: EBIT -35 m USD20222023: 33 m USD2023: EBIT -13 m USD20232024: 28 m USD2024: EBIT -15 m USD20242025: 73 m USD2025: EBIT 31 m USD20257331
RevenueOperating profit (EBIT)

Business

Share of revenue
Drug discovery platform0 %

AI/ML-enabled computational discovery tools used to identify novel targets and pathways.

Proprietary therapeutic programs20 %

Internally developed antibody candidates such as COM902 advanced in clinical development.

Partnered antibody programs80 %

Programs licensed to pharmaceutical partners for development, regulatory and commercial milestones.

Customers

Compugen’s direct customers are primarily pharmaceutical and biotechnology partners that license programs or fund development through collaboration agreements. Its end-market, however, is oncology patients treated through hospitals and cancer centers once partnered or proprietary therapies reach commercialization. The company also serves research and clinical stakeholders who use its discovery platform and programs for target validation and development decisions.

Large pharmaceutical partners

License programs such as COM902-derived assets to fund development, milestones and future royalties.

Biotechnology collaborators

Use the discovery platform and antibody assets to access differentiated cancer immunotherapy programs.

Oncology care providers

Hospitals and cancer centers are the eventual users of approved therapies developed from the pipeline.

Strategy

Compugen’s strategy centers on using its computational discovery platform to generate novel immuno-oncology targets and then advancing a select number of programs internally or with partners. The company also seeks to monetize its science through licensing structures that can deliver upfront payments, milestones and royalties while limiting full commercialization burden.

Advance proprietary pipeline programsMedium term

Internal clinical progress is needed to create future value and strengthen negotiating power with partners.

Leverage partnered programs for non-dilutive economicsShort term

Milestones and royalties can fund discovery work without requiring full commercialization investment.

Use AI/ML discovery to replenish the pipelineLong term

A repeatable discovery engine is essential in a target-rich but highly competitive oncology market.

Geography

Compugen’s corporate and research footprint is centered in Israel, with clinical operations also in the United States. Revenue disclosed in the interim report was entirely from U.S. customers, while Europe showed no revenue in the cited period. The geography matters because discovery and development activities are concentrated in Israel, but commercialization and customer invoicing can be tied to partner and end-customer locations.

Risks

Compugen faces the core risks of a clinical-stage biotech company: pipeline failure, long development timelines and dependence on external partners for commercialization of licensed assets. Revenue is concentrated in collaboration and license economics, so delays in partner progression, trial setbacks or lower-than-expected milestones can materially affect future cash generation.

Sorted by severity
LowMediumHighLowMediumHighImpact →Likelihood →Clinical development risk1Partner concentration and execution risk2Regulatory approval risk3Funding and burn risk4
Impact is the risk’s severity and likelihood how probable it is over the next few years, both assessed from the company’s reports. Numbers match the list.
  1. Clinical development riskImpact: CriticalLikelihood: High

    Pipeline candidates can fail in early or late-stage studies, which would reduce or eliminate future program value.

    Exposure: COM902 and partnered immuno-oncology assets

  2. Partner concentration and execution riskImpact: HighLikelihood: Medium

    A large share of economics depends on AstraZeneca and other partners progressing programs successfully.

    Exposure: Licensed antibody programs and milestone streams

  3. Regulatory approval riskImpact: HighLikelihood: Medium

    Even promising drug candidates require extensive safety and efficacy evidence before approval.

    Exposure: Immuno-oncology pipeline

  4. Funding and burn riskImpact: HighLikelihood: Medium

    Clinical-stage biotech companies typically rely on cash, licensing proceeds and capital markets to fund operations.

    Exposure: R&D and clinical operations

Accounting

Judgemental items
Revenue recognition for licenses and milestones

Collaboration agreements may include upfront, development, regulatory and commercial payments recognized at different times.

Impact: Affects reported revenue timing and deferred revenue balances

Deferred revenue and remaining performance obligations

The company reported deferred revenue and revenue not yet recognized from ongoing obligations.

Impact: Affects visibility into future revenue recognition

Share-based compensation

Equity-based awards are included in segment expense and can materially affect operating results.

Impact: Affects operating expense and non-cash cost structure

Publicly listed companies with a comparable business focus.

Last updated: 28/09/2026