ROIVNasdaqPharmaceutical PreparationsUS GAAP · USD

Roivant Sciences Ltd.

Roivant Sciences Ltd. is a U.S.-based biopharmaceutical company organized around a portfolio of development-stage medicines and technology-enabled subsidiaries, or "Vants." Its business spans drug discovery, clinical development, and eventual commercialization across autoimmune, inflammatory, and pulmonary disease programs, while also incubating complementary health technology and discovery-stage ventures.

Liikevaihto8,3milj. USD
−71,6 %v/v
Liikevoitto (EBIT)−515milj. USD
+48,7 %v/v
EBIT-marginaali−6 235,7%
−2 782,4 %-yks.v/v
Nettotulos−300milj. USD
−74,3 %v/v
Vapaa kassavirta−759milj. USD
+10,1 %v/v

Tilikausi 2026 · muutos edellisvuodesta

Kehitys 2021–2026

−2 00002 0004 0006 000milj. USD2021: 24 milj. USD2021: EBIT −1 071 milj. USD20212022: 55 milj. USD2022: EBIT −1 352 milj. USD20222023: 61 milj. USD2023: EBIT −907 milj. USD20232024: 33 milj. USD2024: EBIT 4 242 milj. USD20242025: 29 milj. USD2025: EBIT −1 003 milj. USD20252026: 8,3 milj. USD2026: EBIT −515 milj. USD20268,3−515
LiikevaihtoLiikevoitto (EBIT)

Liiketoiminta

Osuus liikevaihdosta
Clinical-stage therapeutics70 %

Drug candidates in development for autoimmune, inflammatory, and pulmonary diseases.

Licensing and collaboration revenue20 %

Revenue earned from license agreements and related partnering arrangements.

Subscription and service-based technology revenue10 %

Fees from technology-related subscriptions and services.

Asiakkaat

Roivant's direct counterparties are primarily pharmaceutical and biotechnology partners, licensees, and collaborators that fund or commercialize its programs. Its eventual end customers are patients and prescribers in specialty disease areas such as autoimmune disorders and pulmonary hypertension, reached through approved medicines or partnered commercialization channels.

Pharmaceutical and biotech partners

License and collaboration counterparties that support development, commercialization, or asset monetization.

Patients with autoimmune and inflammatory diseases

End users of therapies such as brepocitinib, IMVT-1402, and batoclimab if approved.

Patients with pulmonary vascular disease

Potential end users of mosliciguat in pulmonary hypertension associated with interstitial lung disease.

Technology and service customers

Subscribers or users of technology-enabled services that generate recurring or service-based revenue.

Strategia

Roivant's strategy is to build and advance a diversified pipeline through small, focused subsidiaries that can move programs efficiently from discovery to commercialization. It also evaluates acquisitions, in-licensing, and capital allocation actions, including share repurchases, to support portfolio growth and optimize its structure.

Advance core clinical programsKeskipitkä aikaväli

Late-stage assets are the main source of future value creation and potential commercialization.

Scale the Vant operating modelKeskipitkä aikaväli

Centralized support and subsidiary autonomy are intended to improve development efficiency.

Optimize capital allocationLyhyt aikaväli

Cash can be used for development, acquisitions, or shareholder returns depending on opportunity set.

Maantiede

Roivant is headquartered in the United States and operates as a global biopharmaceutical platform through subsidiaries and development partners. Its clinical and regulatory exposure is international because product candidates must satisfy FDA and other health-authority requirements before commercialization, and orphan-drug and exclusivity rules differ across the U.S., Europe, and the U.K.

Riskit

Roivant faces the standard risks of biopharmaceutical development: clinical failure, regulatory delay, and uncertainty around commercialization. Its model also depends on successful execution across multiple subsidiaries, partner relationships, and capital-intensive R&D programs, while future value can be affected by patent, exclusivity, and reimbursement dynamics.

Järjestetty vakavuuden mukaan
MatalaKohtalainenKorkeaMatalaKohtalainenKorkeaVaikutus →Todennäköisyys →Regulatory approval risk1Clinical development failure2Commercialization execution risk3Intellectual property and exclusivity risk4Capital allocation and funding risk5
Vaikutus on riskin vakavuus ja todennäköisyys sen toteutumisen todennäköisyys lähivuosina, molemmat arvioitu yhtiön raporttien perusteella. Numerot vastaavat listaa.
  1. Regulatory approval riskVaikutus: KorkeaTodennäköisyys: Korkea

    Medicines cannot be marketed without FDA or other authority approval.

    Kohdistuu: All product candidates

  2. Clinical development failureVaikutus: KorkeaTodennäköisyys: Kohtalainen

    Pipeline value depends on positive trial outcomes for multiple product candidates.

    KohdistuuBrepocitinibIMVT-1402BatoclimabMosliciguat
  3. Commercialization execution riskVaikutus: KeskitasoTodennäköisyys: Kohtalainen

    Launching approved products requires sales, marketing, reimbursement, and distribution capabilities.

    Kohdistuu: Late-stage Vants

  4. Intellectual property and exclusivity riskVaikutus: KeskitasoTodennäköisyys: Kohtalainen

    Future economics depend on patent protection and regulatory exclusivity periods.

    Kohdistuu: Orphan-drug and product exclusivity

  5. Capital allocation and funding riskVaikutus: KeskitasoTodennäköisyys: Matala

    Development programs and acquisitions require substantial capital over time.

    Kohdistuu: Pipeline expansion and in-licensing

Kirjanpito

Harkinnanvaraiset erät
License agreement revenue recognition

Revenue depends on when performance obligations and milestones are satisfied.

Vaikutus: Can create lumpy quarterly revenue

Subscription and service-based revenue

Technology-related fees are recognized as services are delivered or used.

Vaikutus: Affects recurring revenue visibility

Fair value of marketable securities

Investing activity includes purchases and maturities of securities held on balance sheet.

Vaikutus: Can affect other income and liquidity presentation

Discontinued operations and divestiture accounting

Asset sales and exits can change reported revenue, assets, and gains/losses.

Vaikutus: Can distort comparability across periods

Julkisesti listattuja yhtiöitä, joilla on samankaltainen liiketoiminta.

Päivitetty: 24.9.2026

Roivant Sciences Ltd. (ROIV) liikevaihto, tulos ja tunnusluvut 2025 – Clarifo