ACIUNasdaqPharmaceutical PreparationsUS GAAP · USD

AC Immune SA

AC Immune SA is a clinical-stage biopharmaceutical company based in Switzerland that develops medicines and diagnostics for neurodegenerative diseases driven by misfolded proteins. Its work centers on two proprietary platforms, SupraAntigen® and Morphomer®, which it uses to build therapeutic and diagnostic programs for Alzheimer’s disease, Parkinson’s disease, ALS and related indications.

Liikevaihto3,6milj. USD
−86,9 %v/v
Liikevoitto (EBIT)−69,3milj. USD
−32,3 %v/v
EBIT-marginaali−1 940,1%
−1 748,3 %-yks.v/v
Nettotulos−70,4milj. USD
−38,4 %v/v
Vapaa kassavirta−70,2milj. USD
−207,5 %v/v

Tilikausi 2025 · muutos edellisvuodesta

Kehitys 2020–2025

−100−75−50−2502550milj. USD2020: 15 milj. USD2020: EBIT −61 milj. USD20202021: 0,00 milj. USD2021: EBIT −79 milj. USD20212022: 3,9 milj. USD2022: EBIT −71 milj. USD20222023: 15 milj. USD2023: EBIT −54 milj. USD20232024: 27 milj. USD2024: EBIT −52 milj. USD20242025: 3,6 milj. USD2025: EBIT −69 milj. USD20253,6−69
LiikevaihtoLiikevoitto (EBIT)

Liiketoiminta

Osuus liikevaihdosta
Therapeutics - Antibody Programs45 %

Conformation-specific biologics designed to prevent or treat neurodegenerative disease biology.

Therapeutics - Small Molecules20 %

Morphomer-based small-molecule candidates aimed at misfolded protein targets.

Diagnostics15 %

PET and related diagnostic programs intended to detect neurodegenerative pathology.

Collaborations and Licenses20 %

Upfronts, milestones and royalties from partnered development programs.

Asiakkaat

AC Immune’s direct customers are primarily large pharmaceutical partners that license programs, fund development, and may commercialize approved assets. Its end users are patients, clinicians and healthcare systems in neurology and neurodegeneration, where diagnostic clarity and disease-modifying therapies are needed. The company also serves research-oriented collaborators that support platform validation and pipeline advancement.

Pharmaceutical licensing partners

Buy access to discovery programs, development rights and potential commercial rights for lead assets.

Neurology patients and prescribers

Use eventual approved therapies and diagnostics in Alzheimer’s, Parkinson’s and related diseases.

Healthcare imaging providers

Use PET tracers and diagnostic tools to identify pathology and support precision medicine.

Academic and research collaborators

Support preclinical validation, translational work and biomarker development.

Strategia

The company’s strategy is built around a three-pillar model: Alzheimer’s disease, other neurodegenerative diseases such as Parkinson’s and ALS, and diagnostics. It seeks to turn proprietary platform science into partnered and proprietary programs that can attract non-dilutive funding, milestones and royalties while preserving optionality across multiple disease targets.

Advance platform-derived pipeline candidatesLyhyt aikaväli

Clinical validation is the main path to value creation for a platform biopharma company.

Expand partnering and licensing incomeKeskipitkä aikaväli

Upfronts, milestones and royalties reduce funding needs and diversify risk.

Broaden beyond Alzheimer’s diseaseKeskipitkä aikaväli

Multiple indications increase the usable addressable market and platform relevance.

Develop precision diagnosticsPitkä aikaväli

Diagnostics can improve patient selection and support commercialization of therapies.

Maantiede

AC Immune is headquartered in Lausanne, Switzerland and operates through a Swiss parent company with a U.S. subsidiary in Delaware. Its business is global in nature because partnerships, clinical development and intellectual property exploitation span North America, Europe and other major pharmaceutical markets.

Riskit

AC Immune depends on successful clinical development, regulatory clearance and partner execution, all of which are uncertain in neurodegenerative disease. Its revenue model is exposed to collaboration timing and milestone concentration, while its R&D-heavy structure makes capital allocation, trial outcomes and impairment judgments especially important.

Järjestetty vakavuuden mukaan
MatalaKohtalainenKorkeaMatalaKohtalainenKorkeaVaikutus →Todennäköisyys →Clinical development failure1Partner concentration and milestone dependence2Regulatory and trial timeline delays3Funding and dilution risk4Impairment of IPR&D assets5
Vaikutus on riskin vakavuus ja todennäköisyys sen toteutumisen todennäköisyys lähivuosina, molemmat arvioitu yhtiön raporttien perusteella. Numerot vastaavat listaa.
  1. Clinical development failureVaikutus: KriittinenTodennäköisyys: Korkea

    Pipeline value depends on proof of mechanism and clinical efficacy in difficult neurodegenerative diseases.

    Kohdistuu: Phase 2 and Phase 3 assets

  2. Partner concentration and milestone dependenceVaikutus: KorkeaTodennäköisyys: Kohtalainen

    A meaningful part of value creation comes from collaboration agreements and milestone payments.

    Kohdistuu: Licensing and partnership agreements

  3. Regulatory and trial timeline delaysVaikutus: KorkeaTodennäköisyys: Kohtalainen

    Drug and diagnostic approvals require multi-stage testing and agency review.

    Kohdistuu: Therapeutics and diagnostics

  4. Funding and dilution riskVaikutus: KorkeaTodennäköisyys: Kohtalainen

    A clinical-stage biotech typically relies on external capital before product sales emerge.

    Kohdistuu: Cash burn and financing needs

  5. Impairment of IPR&D assetsVaikutus: KeskitasoTodennäköisyys: Kohtalainen

    Capitalized intangibles and development assets can be written down if programs underperform.

    Kohdistuu: Intangible assets

Kirjanpito

Harkinnanvaraiset erät
Revenue recognition for collaborations

Upfront payments, milestones and licensing deliverables may be recognized over time or at points in time.

Vaikutus: Can cause uneven reported revenue

Clinical development accruals

Trial costs are estimated based on work performed by CROs and investigators.

Vaikutus: Can shift expense recognition across periods

IPR&D asset impairment

Development assets depend on scientific and regulatory progress.

Vaikutus: Can create large non-cash charges if programs weaken

Share-based compensation

Equity awards are a meaningful non-cash employee cost for biotech companies.

Vaikutus: Affects operating expenses and equity

Lease accounting

Office and laboratory leases create right-of-use assets and lease liabilities.

Vaikutus: Impacts balance sheet leverage and expense profile

Julkisesti listattuja yhtiöitä, joilla on samankaltainen liiketoiminta.

Päivitetty: 28.9.2026