AAVXFNasdaqPharmaceutical PreparationsUS GAAP · USD

Abivax S.A.

Abivax S.A. is a clinical-stage biotechnology company focused on developing therapeutics that modulate the immune response in chronic inflammatory diseases. It is based in France and the United States and centers on advancing its lead drug candidate, obefazimod (ABX464), through late-stage clinical development.

Liikevaihto0,0milj. USD
Liikevoitto (EBIT)−302milj. USD
−84,2 %v/v
Nettotulos−336milj. USD
−90,7 %v/v
Vapaa kassavirta−161milj. USD
−4,2 %v/v

Tilikausi 2025 · muutos edellisvuodesta

Kehitys 2022–2025

−400−300−200−1000milj. USD2022: 0,00 milj. USD2022: EBIT −54 milj. USD20222023: 0,00 milj. USD2023: EBIT −134 milj. USD20232024: 0,00 milj. USD2024: EBIT −164 milj. USD20242025: 0,00 milj. USD2025: EBIT −302 milj. USD20250,00−302
LiikevaihtoLiikevoitto (EBIT)

Liiketoiminta

Osuus liikevaihdosta
Lead drug candidate100 %

Obefazimod and related development programs for inflammatory diseases.

Asiakkaat

Abivax does not sell commercial products broadly; its direct business counterparties are primarily clinical trial sites, contract research organizations, regulators, and development partners involved in advancing its drug candidates. The ultimate end customers, if approved, are patients with chronic inflammatory diseases such as ulcerative colitis. In practice, the company’s value proposition is tied to demonstrating clinical efficacy and safety that could support future pharmaceutical adoption.

Clinical development partners

CROs, investigators, labs, and manufacturers that execute the development program.

Regulatory stakeholders

Health authorities and ethics committees that assess trial data and approvals.

Patients with inflammatory disease

The intended end users of obefazimod if the therapy reaches commercialization.

Future healthcare payors

Insurers and public health systems that would reimburse treatment use after approval.

Strategia

Abivax’s strategy is centered on advancing obefazimod through late-stage clinical development in ulcerative colitis and building evidence for immune-modulating therapies in chronic inflammatory disease. The company’s competitive position depends on translating clinical data into regulatory progress and, ultimately, a differentiated therapeutic profile. It also maintains the financing and corporate infrastructure needed for a long development cycle.

Complete late-stage clinical developmentLyhyt aikaväli

Clinical readouts are the main value driver for a single-asset biotech company.

Strengthen regulatory positioningLyhyt aikaväli

Approval pathways depend on robust efficacy, safety, and quality data.

Preserve long-duration development capacityKeskipitkä aikaväli

Biotech development requires funding and operating flexibility over multiple years.

Maantiede

Abivax is headquartered in France with a U.S. presence and reports activity tied to both Europe and the United States. Its development operations are therefore exposed to transatlantic clinical, regulatory, and capital market requirements rather than a single national market. The company’s quoted listings in Paris and on Nasdaq also reflect that dual geographic footprint.

Riskit

Abivax faces the typical risks of a clinical-stage biotech company: clinical failure, regulatory delays, and uncertainty around whether trial data will be strong enough for approval. Because its value is concentrated in a small number of programs, any setback in obefazimod or its inflammatory disease pipeline could materially affect the business.

Järjestetty vakavuuden mukaan
MatalaKohtalainenKorkeaMatalaKohtalainenKorkeaVaikutus →Todennäköisyys →Clinical development failure1Regulatory and approval risk4Financing and dilution risk2Pipeline concentration3
Vaikutus on riskin vakavuus ja todennäköisyys sen toteutumisen todennäköisyys lähivuosina, molemmat arvioitu yhtiön raporttien perusteella. Numerot vastaavat listaa.
  1. Clinical development failureVaikutus: KriittinenTodennäköisyys: Kohtalainen

    The company depends on obefazimod progressing successfully through late-stage trials.

    Kohdistuu: Lead candidate in ulcerative colitis

  2. Financing and dilution riskVaikutus: KorkeaTodennäköisyys: Korkea

    Clinical-stage companies often require repeated external capital before commercialization.

    Kohdistuu: Research and development funding

  3. Pipeline concentrationVaikutus: KorkeaTodennäköisyys: Korkea

    The company’s value is concentrated in a limited number of programs and indications.

    Kohdistuu: Obefazimod and inflammatory disease pipeline

  4. Regulatory and approval riskVaikutus: KorkeaTodennäköisyys: Kohtalainen

    Regulators may request further data on efficacy, safety, or manufacturing quality.

    Kohdistuu: Phase 3 and registration pathway

Kirjanpito

Harkinnanvaraiset erät
Research and development expense recognition

Clinical-stage biotech results are heavily affected by when trial and development costs are expensed.

Vaikutus: Affects operating loss and comparability across periods

Fair value measurement of financing instruments

Borrowings, convertible notes, and derivatives may require valuation inputs and remeasurement.

Vaikutus: Can create non-cash volatility in income and liabilities

Estimation uncertainty and judgments

Management must estimate fair values and other balance sheet items with limited observable data.

Vaikutus: Can materially affect reported assets, liabilities, and expense timing

Liability derecognition under IFRS 9

The company adopted a policy change for certain electronic payment settlements.

Vaikutus: Affects timing of liability removal and related financial statement presentation

Julkisesti listattuja yhtiöitä, joilla on samankaltainen liiketoiminta.

Päivitetty: 28.9.2026

Abivax S.A. (Nasdaq) – Pharmaceutical Preparations | Analyysi – Clarifo