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

Immatics N.V.

Immatics N.V. is a clinical-stage biopharmaceutical company focused on discovering and developing T-cell–redirecting cancer immunotherapies. The company works on proprietary TCR-based and bispecific approaches designed to target tumor-associated antigens across multiple solid tumor indications, with operations spanning Europe and the United States through its corporate group.

Revenue48.3m USD
−69.0 %y/y
Operating profit (EBIT)-197m USD
−988.3 %y/y
EBIT margin-409.2%
−423.4 ppy/y
Net income-196m USD
−1,390.9 %y/y
Free cash flow-183m USD
−5.1 %y/y

Fiscal year 2025 · change from previous year

Development 2022–2025

-200-1000100200m USD2022: 173 m USD2022: EBIT 43 m USD20222023: 54 m USD2023: EBIT -96 m USD20232024: 156 m USD2024: EBIT 22 m USD20242025: 48 m USD2025: EBIT -197 m USD202548-197
RevenueOperating profit (EBIT)

Business

Share of revenue
TCR-based immunotherapies50 %

Engineered therapies that use T-cell receptors to recognize tumor antigens.

Bispecific antibody programs20 %

T-cell–redirecting molecules designed to engage immune cells against tumors.

Research collaborations and licensing15 %

Partnered research, development, and licensing activities around oncology targets.

Preclinical discovery programs15 %

Target identification and early-stage validation work for future drug candidates.

Customers

Immatics does not sell a conventional commercial product portfolio; its primary counterparties are pharmaceutical partners, research collaborators, and clinical trial sites. Its programs are ultimately aimed at patients with solid tumors, but near-term economic activity is driven by collaboration structures, development agreements, and clinical research relationships.

Pharmaceutical partners

Buy access to proprietary targets, therapeutic candidates, or collaboration rights for oncology development.

Biotech collaborators

Engage in platform or program collaborations to expand their immuno-oncology pipelines.

Clinical trial sites

Run studies and provide patient recruitment and data generation for pipeline programs.

Patients in oncology trials

Receive experimental therapies in solid tumor studies as part of clinical development.

Research institutions

Support target discovery, biomarker work, and translational research around tumor antigens.

Strategy

Immatics’ strategy centers on advancing T-cell redirecting therapies from discovery into clinical proof-of-concept, with emphasis on tumor antigens that can support multiple solid tumor programs. The company also uses collaborations and partnering to extend its platform, share development risk, and broaden the reach of its antigen-discovery capabilities.

Clinical advancement of core programsShort term

Human data are needed to validate the platform and support partnering or internal development.

Target and biomarker differentiationMedium term

Unique antigen presentation and patient-selection logic can improve therapeutic specificity.

Partnership-driven development modelMedium term

Collaborations can provide capital, expertise, and external validation for pipeline assets.

Geography

Immatics is organized as a cross-border biopharmaceutical group with roots in Europe and a corporate presence in the United States. Its research, development, and investor-relations footprint spans multiple countries, while clinical development is conducted through international trial networks rather than a single domestic market.

Risks

As a clinical-stage oncology company, Immatics faces substantial development risk because its programs must show safety, target engagement, and efficacy in humans before becoming commercially viable. The business also depends on capital access, scientific differentiation, and complex accounting estimates tied to R&D and share-based compensation.

Sorted by severity
LowMediumHighLowMediumHighImpact →Likelihood →Clinical development failure1Scientific and target-validation risk2Financing and partner-dependence risk3Competition in oncology immunotherapy4
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 failureImpact: CriticalLikelihood: High

    Programs must demonstrate safety and efficacy in patients, and oncology trials often fail in later stages.

    Exposure: Lead TCR and bispecific programs

  2. Scientific and target-validation riskImpact: HighLikelihood: High

    Therapies rely on tumor antigen presentation and immune recognition that may not translate consistently across patients.

    Exposure: TCR-based platform and biomarker strategy

  3. Financing and partner-dependence riskImpact: HighLikelihood: High

    Clinical-stage biopharma typically needs external funding and collaboration revenue to sustain development.

    Exposure: Research and clinical pipeline funding

  4. Competition in oncology immunotherapyImpact: MediumLikelihood: High

    Multiple companies are pursuing T-cell redirection, making differentiation and deal access important.

    Exposure: Pipeline positioning and partnering

Accounting

Judgemental items
Revenue recognition

Collaboration and licensing arrangements may require allocation across performance obligations and milestones.

Impact: Can shift revenue timing between periods

Research and development expenses

Clinical and preclinical spending must be classified and accrued based on project stage and vendor estimates.

Impact: Affects operating loss and comparability

Share-based compensation

Equity awards to employees create non-cash expense that can be material for a biotech company.

Impact: Influences reported personnel costs and loss

Income taxes and deferred tax judgments

Cross-border operations and loss carryforwards require estimation of tax assets and liabilities.

Impact: Can affect the balance sheet and net loss

Publicly listed companies with a comparable business focus.

Last updated: 28/09/2026