Pharmaceutical PreparationsIFRS · EUR

RAPT Therapeutics, Inc.

RAPT Therapeutics, Inc. is a U.S.-based clinical-stage biopharmaceutical company focused on discovering and developing small-molecule therapies for inflammatory and immunological diseases and cancer. The company’s work centers on drug candidates intended for use in areas such as immunology, inflammation, and oncology, with development activities conducted through its corporate research and clinical organization in the United States.

Operating profit (EBIT)-136m EUR
−7.1 %y/y
Net income-130m EUR
−11.2 %y/y
Free cash flow-83.4m EUR
+15.0 %y/y

Fiscal year 2024 · change from previous year

Development 2019–2024

-150-100-50050m EUR2019: EBIT -44 m EUR20192020: 5.0 m EUR2020: EBIT -53 m EUR20202021: 3.8 m EUR2021: EBIT -69 m EUR20212022: 1.5 m EUR2022: EBIT -86 m EUR20222023: 0.00 m EUR2023: EBIT -127 m EUR20232024: EBIT -136 m EUR2024-136
RevenueOperating profit (EBIT)

Business

Share of revenue
Inflammation and immunology programs50 %

Drug discovery and development efforts targeting inflammatory and immune-mediated diseases.

Oncology programs35 %

Therapeutic candidates and research programs aimed at cancer indications.

Preclinical research15 %

Early-stage discovery, screening, and translational work supporting the pipeline.

Customers

RAPT does not currently sell commercial products; its near-term counterparties are primarily clinical investigators, contract research organizations, manufacturers, regulators, and potential development partners. If any candidate is approved, the end customers would be physicians, hospitals, and payors that influence adoption and reimbursement in the U.S. healthcare system.

Clinical development partners

CROs, trial sites, and manufacturers that support testing and supply of drug candidates.

Potential strategic partners

Biopharma companies that may license, co-develop, or commercialize candidates.

Healthcare providers

Physicians and hospitals that would prescribe or administer approved therapies.

Third-party payors

Insurers and government payors that determine coverage and reimbursement.

Strategy

RAPT’s strategy is to advance its pipeline through preclinical and clinical development, using external partners where needed for research, manufacturing, and trial execution. The company also emphasizes maintaining intellectual property protection and preserving optionality for future financing, collaborations, or licensing transactions that could support development and eventual commercialization.

Advance pipeline candidatesShort term

Clinical and preclinical progress is the main value driver for a therapeutics company with no product revenue.

Secure development and commercialization partnersMedium term

The company lacks internal sales and distribution capabilities and may need third parties to bring products to market.

Maintain funding runwayShort term

Ongoing R&D and clinical work require external capital until product revenue exists, if ever.

Geography

RAPT is headquartered and operates in the United States, where its research, clinical development, and corporate functions are centered. Its business is also exposed to global clinical-trial, manufacturing, and regulatory dependencies, since trials, suppliers, and future commercialization could involve non-U.S. counterparties and jurisdictions.

Risks

RAPT faces the typical risks of a clinical-stage biotech company: pipeline failure, long development timelines, regulatory uncertainty, and dependence on external funding. Its future commercial success also depends on reimbursement, intellectual property protection, supply chain reliability, and the ability to build or outsource sales and distribution capabilities if a product is approved.

Sorted by severity
LowMediumHighLowMediumHighImpact →Likelihood →Clinical development failure or delay1Funding and liquidity dependence2Supply chain and regulatory disruption3Commercialization capability gap4Competition and IP risk5Reimbursement and pricing pressure6
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 failure or delayImpact: HighLikelihood: High

    Drug candidates may not show sufficient safety or efficacy, or trials may take longer than planned.

    ExposurePipeline programs in inflammationImmunologyOncology
  2. Funding and liquidity dependenceImpact: HighLikelihood: High

    The company expects to need substantial additional capital before generating product revenue.

    ExposureEquityDebtCollaborationsStrategic transactions
  3. Supply chain and regulatory disruptionImpact: MediumLikelihood: High

    Clinical trials depend on CROs, manufacturers, and FDA/regulatory operations.

    ExposureTrial sitesManufacturingApprovals
  4. Commercialization capability gapImpact: MediumLikelihood: Medium

    RAPT currently has no sales, marketing, or distribution infrastructure.

    Exposure: Future approved products

  5. Competition and IP riskImpact: MediumLikelihood: Medium

    Larger, better funded biotech and pharma companies may develop superior or earlier therapies.

    ExposureInflammationImmunologyOncology markets
  6. Reimbursement and pricing pressureImpact: MediumLikelihood: Low

    Payors may restrict coverage, require discounts, or demand additional evidence.

    Exposure: U.S. pharmaceutical commercialization

Accounting

Judgemental items
Research and development expense recognition

External trial, lab, and manufacturing costs are expensed as incurred, affecting quarterly comparability.

Impact: Reported operating loss

Marketable securities and interest income

Cash is invested in money market funds, corporate debt, commercial paper, and agency securities.

Impact: Other income, net

Prepaid R&D services

Non-refundable advance payments are recognized as expense when goods or services are received.

Impact: Timing of operating expenses

Future collaboration or licensing revenue

Any partnering deal could require judgment on performance obligations and revenue timing.

Impact: Potential future revenue recognition

Publicly listed companies with a comparable business focus.

Last updated: 24/09/2026