APLMWNasdaqPharmaceutical PreparationsUS GAAP · USD

Apollomics Inc.

Apollomics Inc. is a U.S.-based clinical-stage biopharmaceutical company focused on discovering and developing oncology therapies. Its lead asset is vebreltinib (APL-101), a c-Met inhibitor being developed for non-small cell lung cancer and other advanced tumors with c-Met alterations, with development activity in the United States and international markets outside Mainland China and Macau.

Revenue8.5m USD
Operating profit (EBIT)-10.9m USD
+79.6 %y/y
EBIT margin-127.9%
Net income-10.9m USD
+79.7 %y/y
Free cash flow-10.4m USD
+64.0 %y/y

Fiscal year 2025 · change from previous year

Development 2022–2025

-250-200-150-100-50050m USD2022: 0.00 m USD2022: EBIT -241 m USD20222023: 0.00 m USD2023: EBIT -172 m USD20232024: 0.00 m USD2024: EBIT -53 m USD20242025: 8.5 m USD2025: EBIT -11 m USD20258.5-11
RevenueOperating profit (EBIT)

Business

Share of revenue
Lead clinical program100 %

Development of vebreltinib (APL-101), a selective c-Met inhibitor for cancer.

Oncology licensing and collaboration0 %

Out-licensing and regional development rights for vebreltinib in selected territories.

Clinical-stage research and development0 %

Pre-commercial research, clinical trials, and regulatory development activities.

Customers

Apollomics does not sell broadly to end consumers; its economic counterparties are licensing partners, clinical investigators, hospitals, and trial sites supporting drug development. In commercial terms, value is created through regional partnering arrangements for vebreltinib and future oncology collaborations rather than mass-market product sales.

Licensing partners

Pharmaceutical partners that acquire regional rights to develop and commercialize vebreltinib.

Clinical trial sites

Hospitals and research centers that administer studies and enroll patients.

Oncology patients

Patients with non-small cell lung cancer or other c-Met altered tumors enrolled in trials.

Future commercialization partners

Potential partners that may support later-stage development and market access.

Strategy

Apollomics’ strategy centers on advancing vebreltinib through clinical development while retaining broad control over ex-China rights. The company also seeks to use regional partnerships to extend reach, fund development, and preserve flexibility for future commercialization opportunities.

Advance vebreltinib clinicallyShort term

Clinical data and regulatory progress determine the asset's long-term value.

Partner regional rightsMedium term

Licensing can provide non-dilutive capital and local market expertise.

Preserve ex-China controlMedium term

Maintaining ownership across key markets increases flexibility for future deals.

Geography

Apollomics is headquartered in the United States and develops vebreltinib across the U.S., Europe, and the broader Asia-Pacific region. The company has retained rights outside Mainland China and Macau, so its commercial footprint is shaped by regional licensing, clinical trial execution, and partner-dependent expansion across multiple jurisdictions.

Risks

Apollomics faces the classic risks of a clinical-stage biotech company: trial failure, regulatory delay, and dependence on external capital and partners. The company also has geographic and contractual exposure because its lead asset is monetized through regional rights and collaborations, making execution and partner quality important to future value creation.

Sorted by severity
LowMediumHighLowMediumHighImpact →Likelihood →Clinical development failure1Partner execution risk3Financing dependence2Regulatory and trial timing 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 failureImpact: CriticalLikelihood: Medium

    Vebreltinib is still in clinical development and may not achieve efficacy or safety targets.

    Exposure: Lead asset vebreltinib

  2. Financing dependenceImpact: HighLikelihood: High

    Clinical-stage biopharma companies typically require repeated external funding to support trials and operations.

    Exposure: Working capital and development funding

  3. Partner execution riskImpact: HighLikelihood: Medium

    Regional licensing and commercialization outcomes depend on counterparties' diligence and investment.

    Exposure: Asia and future ex-China partnerships

  4. Regulatory and trial timing riskImpact: MediumLikelihood: High

    Drug development timelines are vulnerable to FDA and ex-U.S. review processes.

    ExposureU.SEuropeAsia-Pacific development

Accounting

Judgemental items
Licensing revenue recognition

Upfront payments from regional agreements affect when revenue is recorded and can create lumpy periods.

Impact: 2025 revenue was tied to an Asia licensing upfront payment

Intangible asset impairment

Development assets require periodic recoverability testing and may be written down if prospects weaken.

Impact: Impairment charges affected reported loss

Fair value measurement

Valuation of financial assets, liabilities, and convertible instruments can affect profit or loss.

Impact: Non-cash gains and losses may distort comparability

Convertible note accounting

Bridge financing with conversion features requires assessment of liability and equity treatment.

Impact: Can influence balance sheet classification and dilution

Publicly listed companies with a comparable business focus.

Last updated: 28/09/2026