STTKNasdaqPharmaceutical PreparationsUS GAAP · USD

Shattuck Labs, Inc.

Shattuck Labs is a U.S.-based clinical-stage biotechnology company focused on discovering and developing antibody-based therapies for immune-mediated diseases. The company’s pipeline has centered on programs such as SL-325 and earlier candidates, with research, development, and clinical operations conducted from its U.S. offices in Austin, Texas and Durham, North Carolina.

Revenue1.0m USD
−82.5 %y/y
Operating profit (EBIT)-51.5m USD
+36.1 %y/y
EBIT margin-5,150.8%
−3,742.5 ppy/y
Net income-48.8m USD
+35.3 %y/y
Free cash flow-40.0m USD
+34.0 %y/y

Fiscal year 2025 · change from previous year

Development 2020–2025

-150-100-50050m USD2020: 9.9 m USD2020: EBIT -37 m USD20202021: 30 m USD2021: EBIT -45 m USD20212022: 0.65 m USD2022: EBIT -103 m USD20222023: 1.7 m USD2023: EBIT -92 m USD20232024: 5.7 m USD2024: EBIT -81 m USD20242025: 1.0 m USD2025: EBIT -52 m USD20251.0-52
RevenueOperating profit (EBIT)

Business

Share of revenue
Clinical-stage drug candidates70 %

Antibody-based therapeutic programs being advanced through preclinical and clinical development.

Collaboration and license revenue20 %

Revenue from research, licensing, and collaboration agreements with third parties.

Discovery and translational research10 %

Internal research activities that generate new therapeutic candidates and platform insights.

Customers

Shattuck Labs does not sell approved commercial products; its economic counterparties are pharmaceutical and biotechnology partners, research collaborators, and potential future licensing or development partners. Its programs are aimed at patients with immune-mediated diseases, while current revenue is tied to collaboration and license agreements rather than product sales.

Pharmaceutical and biotechnology collaborators

Partners that enter research, option, or license agreements around Shattuck’s antibody programs and platform assets.

Clinical development partners

Organizations that may support or co-develop later-stage trials, manufacturing, or commercialization.

Patients with immune-mediated diseases

The eventual end users of approved therapies targeting inflammatory and immune-mediated conditions.

Strategy

The company’s strategy is to advance antibody programs for immune-mediated diseases, with emphasis on clinical development of SL-325 and related pipeline assets. It also seeks to balance internal scientific capability with outsourced clinical research and manufacturing, while preserving flexibility to fund development through collaborations and capital raises.

Advance SL-325 into later-stage developmentShort term

Clinical progress is the main value driver for a company without commercial products.

Strengthen internal development capabilitiesMedium term

More in-house expertise can improve execution in research, process development, and clinical operations.

Use partnerships to extend capital runway and broaden reachMedium term

Collaborations can provide non-dilutive funding and external validation of the platform.

Geography

Shattuck Labs is headquartered and operates in the United States, with corporate offices in Austin, Texas and Durham, North Carolina. Its research and development footprint is U.S.-based, while clinical and manufacturing activities are outsourced to third-party organizations that may operate in multiple jurisdictions.

Risks

Shattuck Labs faces the typical risks of a clinical-stage biotech company: uncertain trial outcomes, regulatory approval risk, and dependence on external funding before any commercial product exists. Its business also depends on third-party CROs and contract manufacturers, making execution, supply, and quality control important sources of risk.

Sorted by severity
LowMediumHighLowMediumHighImpact →Likelihood →Clinical development failure1Intellectual property protection4Capital dependence2Third-party manufacturing and trial execution3Competitive pressure5
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: Medium

    Product candidates may not show sufficient safety or efficacy in trials.

    Exposure: SL-325 and other immune-mediated disease programs

  2. Capital dependenceImpact: HighLikelihood: High

    The company has no commercial product revenue and must fund long development cycles.

    Exposure: Operating runway and trial funding

  3. Third-party manufacturing and trial executionImpact: HighLikelihood: High

    CROs and contract manufacturers control key parts of development and supply.

    ExposureClinical timelinesQualityMaterial availability
  4. Intellectual property protectionImpact: HighLikelihood: Medium

    Patent coverage is needed to protect candidate molecules, methods, and formulations.

    Exposure: Platform technology and lead programs

  5. Competitive pressureImpact: MediumLikelihood: Medium

    Larger companies and other clinical-stage peers are pursuing similar immune targets.

    Exposure: TL1A/DR3-axis and broader immune-mediated disease space

Accounting

Judgemental items
Revenue recognition for collaboration agreements

Revenue is recognized as performance obligations are satisfied, so timing can be uneven across periods.

Impact: Affects reported quarterly and annual revenue

Accrued research and development expenses

The company relies on third parties for trials and manufacturing, requiring estimates for unpaid services.

Impact: Affects operating expenses and liabilities

Stock-based compensation

Equity awards are a meaningful part of employee compensation and require valuation assumptions.

Impact: Affects operating expense and dilution analysis

Publicly listed companies with a comparable business focus.

Last updated: 24/09/2026

Shattuck Labs, Inc. (Nasdaq) – Pharmaceutical Preparations | Financial Analysis – Clarifo