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

Compass Therapeutics, Inc.

Compass Therapeutics is a clinical-stage biopharmaceutical company focused on developing antibody-based cancer therapies. Its pipeline centers on bispecific and other proprietary antibodies designed to disrupt angiogenesis and tumor biology, with lead programs including tovecimig, CTX-471, CTX-8371, and CTX-10726.

Revenue0.0m USD
−100.0 %y/y
Operating profit (EBIT)-72.8m USD
−28.6 %y/y
Net income-66.5m USD
−34.7 %y/y
Free cash flow-49.2m USD
−9.5 %y/y

Fiscal year 2025 · change from previous year

Development 2020–2025

-100-80-60-40-20020m USD2020: EBIT -28 m USD20202021: EBIT -82 m USD20212022: EBIT -42 m USD20222023: 0.00 m USD2023: EBIT -50 m USD20232024: 0.85 m USD2024: EBIT -57 m USD20242025: 0.00 m USD2025: EBIT -73 m USD20250.00-73
RevenueOperating profit (EBIT)

Business

Share of revenue
Clinical-stage oncology programs85 %

Lead and follow-on antibody candidates being advanced through clinical and IND-enabling development.

Platform technology10 %

StitchMabsTM and related antibody discovery/engineering capabilities used to create bispecifics.

Licensing and collaboration revenue5 %

Milestones and other payments from partners for licensed product rights and development progress.

Customers

Compass Therapeutics does not yet sell approved products; its current economic counterparties are licensing partners, contract manufacturers, and clinical research vendors. If approved, its end customers would be physicians, hospitals, and third-party payors that influence adoption and reimbursement of oncology therapies.

Licensing and collaboration partners

Biopharma partners that pay milestones or royalties for rights to selected programs or geographies.

Clinical trial ecosystem

Hospitals, investigators, CROs, and vendors that support development of product candidates.

Future oncology prescribers

Physicians and cancer centers that would use approved products if the pipeline reaches market.

Third-party payors

Insurers and reimbursement bodies that would influence uptake and net access after approval.

Strategy

The company is focused on advancing its antibody pipeline through clinical development while preserving optionality to partner selected rights by geography or program. Management also emphasizes capital discipline, noting that current cash is expected to fund operations into 2028, but additional financing or strategic transactions may still be needed to support development and eventual commercialization.

Advance the clinical pipelineShort term

Clinical data and regulatory progress are the main value drivers for a pre-revenue biotech.

Maintain partnering optionalityMedium term

Regional or program-level deals can fund development and reduce capital burden.

Extend cash runwayShort term

The company expects to need substantial additional funding before product sales.

Geography

Compass Therapeutics is headquartered in Boston, Massachusetts and operates as a U.S.-based clinical-stage company with worldwide rights to most of its programs. The company relies on third-party manufacturers and research partners, and it has disclosed a China-linked milestone from Elpiscience tied to a Phase 1 trial, showing that development and partnering can extend beyond the U.S.

Risks

Compass Therapeutics is a pre-commercial biotech with no approved products, so its value depends on successful clinical development, regulatory clearance, and eventual market adoption. It also depends heavily on third parties for trials and manufacturing, and it faces typical oncology-biotech risks such as capital needs, intellectual property competition, and cybersecurity exposure.

Sorted by severity
LowMediumHighLowMediumHighImpact →Likelihood →No products approved for commercial sale1Need for additional capital2Third-party trial and manufacturing dependence3Cybersecurity and data privacy4
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. No products approved for commercial saleImpact: CriticalLikelihood: High

    The company has a limited operating history and depends on pipeline success to create revenue.

    Exposure: Entire business model

  2. Need for additional capitalImpact: HighLikelihood: High

    R&D spending exceeds revenue and the company may need equity, debt, or partnerships to fund operations.

    Exposure: Cash runway and development continuity

  3. Third-party trial and manufacturing dependenceImpact: HighLikelihood: Medium

    The company relies on CROs and contract manufacturers for clinical studies and supply.

    Exposure: Development timelines and regulatory readiness

  4. Cybersecurity and data privacyImpact: MediumLikelihood: Low

    Research data, IP, and personal information are stored digitally and may be targeted or disrupted.

    Exposure: Confidential data and operational continuity

  5. Intellectual property competitionImpact: Medium

    Biotech competitors and larger pharma companies may develop similar oncology assets or challenge IP.

    Exposure: Pipeline differentiation and partnering leverage

Accounting

Judgemental items
Research and development expense accruals

Management estimates progress on outsourced work, which affects current-period expense and liabilities.

Impact: Can shift expense timing between periods

Milestone-based licensing revenue

Revenue depends on achievement of contractual milestones, creating lumpy and non-recurring recognition.

Impact: Can materially affect quarterly comparability

Stock-based compensation

Equity awards are a meaningful operating cost for a development-stage biotech.

Impact: Affects operating loss and non-cash expense profile

Operating lease commitments

Boston office and laboratory leases create fixed obligations and disclosure requirements.

Impact: Affects liquidity analysis and future cash outflows

Publicly listed companies with a comparable business focus.

Last updated: 24/09/2026