HMDCFNasdaqPharmaceutical PreparationsUS GAAP · USD

HUTCHMED (China) Ltd

HUTCHMED (China) Ltd is a biopharmaceutical company focused on discovering, developing, and commercializing targeted therapies and immunotherapies for cancer and immunological diseases. It has operations spanning China and international markets, with products and development programs supported by in-house R&D, third-party partners, and manufacturing arrangements.

Liikevaihto549milj. USD
−13,0 %v/v
Liikevoitto (EBIT)−39,2milj. USD
+10,4 %v/v
EBIT-marginaali−7,1%
−0,2 %-yks.v/v
Nettotulos457milj. USD
+1 111,0 %v/v
Vapaa kassavirta−78,8milj. USD
−352,0 %v/v

Tilikausi 2025 · muutos edellisvuodesta

Kehitys 2020–2025

−500−25002505007501 000milj. USD2020: 228 milj. USD2020: EBIT −197 milj. USD20202021: 356 milj. USD2021: EBIT −328 milj. USD20212022: 426 milj. USD2022: EBIT −408 milj. USD20222023: 838 milj. USD2023: EBIT 18 milj. USD20232024: 630 milj. USD2024: EBIT −44 milj. USD20242025: 549 milj. USD2025: EBIT −39 milj. USD2025549−39
LiikevaihtoLiikevoitto (EBIT)

Liiketoiminta

Osuus liikevaihdosta
Commercial oncology medicines55 %

Approved cancer drugs sold through partners or direct supply channels.

Clinical-stage oncology pipeline25 %

Investigational cancer therapies in global and China development.

Immunology pipeline10 %

Drug candidates for immunological diseases and related research programs.

Distribution business and other ventures10 %

Third-party pharmaceutical distribution and other non-core activities in China.

Tuotteet

Raportoitu · osuus liikevaihdosta
47,9%18,3%12,5%FY2025100 %
  • Goods Distribution47,9 %
  • Marketed Products18,3 %
  • Other Collaboration Royalties Revenue12,5 %
  • Commercialization Services8,3 %
  • License and Collaborations Manufacturing Supply5,7 %
  • Muut7,3 %

Lähde: 20-F FY2025, yhtiön tuotelinjoittain raportoima liikevaihto (SEC XBRL). Osuudet on laskettu näytetyistä riveistä ja ne summautuvat 100 %:iin.

Asiakkaat

Customers include hospitals, physicians, and patients accessing approved oncology medicines in China and other markets through commercial channels and partners. The company also serves pharmaceutical partners and distributors through its distribution venture, as well as clinical investigators and trial sites involved in its development programs.

Hospitals and oncologists

Buy or prescribe approved oncology drugs for patients with cancer.

Patients and caregivers

End users of commercialized medicines, accessed through healthcare providers and reimbursement channels.

Pharmaceutical partners

License, co-develop, or commercialize selected assets in defined geographies.

Clinical trial investigators and sites

Use investigational products supplied for global and China studies.

Third-party pharmaceutical customers in China

Use distribution services provided through the joint venture business.

Strategia

The company’s strategy is to advance internally discovered oncology assets from research into commercialization, using partnerships to broaden reach while retaining key territorial rights where strategically important. It also supports this model with manufacturing control for selected products and with a distribution venture that adds non-core operating income in China.

Advance targeted oncology pipelineKeskipitkä aikaväli

Late-stage and earlier programs can expand the marketed portfolio and create future partnered or self-commercialized products.

Protect and expand territorial rightsKeskipitkä aikaväli

Retaining rights in Mainland China and nearby markets preserves strategic value in the company’s core geography.

Strengthen manufacturing and supply chainLyhyt aikaväli

In-house and outsourced manufacturing support commercialization, supply continuity, and global launch readiness.

Leverage partnerships for market accessKeskipitkä aikaväli

Commercial partners can broaden geographic reach and reduce the burden of direct commercialization.

Maantiede

HUTCHMED’s business is centered on China, where its marketed products and distribution activities are concentrated, while its development and commercialization footprint extends to Hong Kong, Macau, Taiwan, the U.S., Europe, and Japan. Manufacturing is anchored in Shanghai, with additional commercial supply supported by a third-party CDMO site in Switzerland for certain products.

Riskit

HUTCHMED’s risk profile is shaped by drug development uncertainty, regulatory approval dependence, and commercialization execution in highly competitive oncology markets. The business also faces manufacturing, partner, and reimbursement risks because much of its value depends on successful trials, regulatory clearances, and third-party commercial relationships.

Järjestetty vakavuuden mukaan
MatalaKohtalainenKorkeaMatalaKohtalainenKorkeaVaikutus →Todennäköisyys →Clinical development failure1Regulatory approval and compliance risk2Partner dependence3Reimbursement and pricing pressure4Manufacturing and supply disruption5
Vaikutus on riskin vakavuus ja todennäköisyys sen toteutumisen todennäköisyys lähivuosina, molemmat arvioitu yhtiön raporttien perusteella. Numerot vastaavat listaa.
  1. Clinical development failureVaikutus: KorkeaTodennäköisyys: Kohtalainen

    Drug candidates may not demonstrate sufficient safety or efficacy in trials, which can eliminate expected product value.

    Kohdistuu: Pipeline oncology and immunology assets

  2. Regulatory approval and compliance riskVaikutus: KorkeaTodennäköisyys: Kohtalainen

    Commercialization depends on approvals and manufacturing inspections across multiple jurisdictions.

    KohdistuuChinaU.SEuropeJapan
  3. Partner dependenceVaikutus: KorkeaTodennäköisyys: Kohtalainen

    Some key products are marketed or developed with partners, so execution and economics depend on third parties.

    KohdistuuAstraZenecaGSKOther collaborators
  4. Reimbursement and pricing pressureVaikutus: KeskitasoTodennäköisyys: Korkea

    Market access for oncology medicines can be affected by inclusion in reimbursement formularies and pricing negotiations.

    Kohdistuu: China commercial market

  5. Manufacturing and supply disruptionVaikutus: KeskitasoTodennäköisyys: Kohtalainen

    Commercial supply relies on Shanghai production and select external CDMO capacity.

    KohdistuuShanghai facilitySwitzerland CDMO

Kirjanpito

Harkinnanvaraiset erät
License and milestone revenue

Upfront, regulatory, and commercial milestone payments may be recognized at different times, affecting comparability across periods.

Vaikutus: Can create lumpy revenue and earnings

Royalty accounting

Partner commercialization can generate royalties tied to third-party net sales, making revenue dependent on external sales performance.

Vaikutus: Variable revenue stream

Joint venture consolidation and disposals

The distribution business and equity interest disposals can materially change reported earnings and revenue mix.

Vaikutus: Affects non-core income and margins

Clinical development expenditure

Research and development costs are typically incurred before revenue is realized, influencing operating results.

Vaikutus: Drives expense intensity

Foreign currency translation

The company operates across currencies and jurisdictions, so translation effects can move comprehensive income.

Vaikutus: Impacts equity and OCI

Julkisesti listattuja yhtiöitä, joilla on samankaltainen liiketoiminta.

Päivitetty: 28.9.2026

HUTCHMED (China) Ltd (HMDCF) liikevaihto, tulos ja tunnusluvut 2025 – Clarifo