MTVANasdaqPharmaceutical PreparationsUS GAAP · USD

MetaVia Inc.

MetaVia Inc. is a clinical-stage biotechnology company developing novel pharmaceuticals for cardiometabolic diseases. Its current pipeline is focused on two programs targeting metabolic dysfunction-associated steatohepatitis (MASH) and obesity, with R&D spending centered on advancing those product candidates through clinical development.

Liikevoitto (EBIT)−13,7milj. USD
+52,4 %v/v
Nettotulos−13,0milj. USD
+53,0 %v/v
Vapaa kassavirta−15,7milj. USD
+36,5 %v/v

Tilikausi 2025 · muutos edellisvuodesta

Kehitys 2020–2025

−30−20−100milj. USD2020: EBIT −30 milj. USD20202021: EBIT −15 milj. USD20212022: EBIT −20 milj. USD20222023: EBIT −16 milj. USD20232024: EBIT −29 milj. USD20242025: EBIT −14 milj. USD2025−14
LiikevaihtoLiikevoitto (EBIT)

Liiketoiminta

Osuus liikevaihdosta
Lead clinical programs0 %

Core pipeline assets under development for MASH and obesity, including Vanoglipel (DA-1241) and DA-1726.

Research and development services100 %

Internal and outsourced R&D activities such as CRO work, consultants, and clinical operations.

Manufacturing and supply chain support0 %

Drug product manufacturing, storage, and CMO-related services used for preclinical and clinical studies.

Licensing and collaboration arrangements0 %

Third-party licensing and shared-services arrangements that support development programs.

Asiakkaat

MetaVia does not sell commercial medicines yet; its primary stakeholders are clinical investigators, CROs, CMOs, and licensing partners that enable drug development. The eventual end customers would be physicians and patients in cardiometabolic disease markets, but near-term value creation depends on advancing the pipeline and securing financing or collaboration support.

Clinical development vendors

CROs, consultants, and trial operators that execute studies and provide development expertise.

Manufacturing partners

CMOs and related suppliers that make and store drug product for preclinical and clinical use.

Licensing and collaboration partners

Third parties such as Dong-A ST that provide shared services, rights, or funding support.

Future prescribers and patients

Physicians and patients in MASH and obesity markets who would use approved therapies if development succeeds.

Strategia

MetaVia's near-term strategy is to conserve capital while advancing its MASH and obesity programs through clinical development. Management also expects to supplement cash through equity, debt, or collaboration structures, which makes financing execution as important as scientific progress.

Advance the MASH and obesity pipelineLyhyt aikaväli

Clinical progress is the main driver of future value and partnering optionality.

Secure additional financingLyhyt aikaväli

The company expects current cash to fund operations only into 2026 and may need more capital to continue trials.

Manage development spend and runwayKeskipitkä aikaväli

R&D is the primary cash use, so disciplined spending determines how long the pipeline can progress.

Maantiede

MetaVia is a U.S.-based company and reports under U.S. GAAP, with operations centered on development activities rather than a broad commercial footprint. The excerpts provided do not disclose country-level revenue, which is consistent with a clinical-stage business that has not yet built a commercial sales base.

Riskit

MetaVia faces the typical risks of a clinical-stage biotech company: clinical failure, regulatory setbacks, and dependence on external capital. Its going-concern language, limited cash runway, and reliance on equity financing make dilution and trial delays material business risks.

Järjestetty vakavuuden mukaan
Clinical development failureKriittinen

Pipeline value depends on successful outcomes for Vanoglipel and DA-1726.

Kohdistuu: MASH and obesity programs

Going-concern and liquidity riskKorkea

The company states it expects cash to fund operations only into 2026 and may need additional capital.

Kohdistuu: Clinical trials and corporate operations

Dilution from equity financingKorkea

Operations have been funded primarily through equity offerings and convertible securities.

Kohdistuu: Existing shareholders

Regulatory and trial execution riskKeskitaso

Clinical-stage companies depend on approvals, site execution, and compliance with regulatory requirements.

KohdistuuCROsCMOsTrial operations

Kirjanpito

Harkinnanvaraiset erät
Warrant liability fair value

Changes in warrant valuation flow through earnings and can create non-cash volatility.

Vaikutus: Other income/expense

Stock-based compensation

Employee awards are a recurring non-cash cost and part of R&D overhead.

Vaikutus: Operating expenses and net loss

Accrued expenses

Management must estimate unpaid clinical, consulting, and manufacturing costs at period end.

Vaikutus: Operating liabilities and expense timing

R&D expense recognition

Clinical development, CMO, CRO, and regulatory costs are expensed as incurred, affecting comparability quarter to quarter.

Vaikutus: Reported operating loss

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Päivitetty: 28.4.2026

MetaVia Inc. (Nasdaq) – Pharmaceutical Preparations | Analyysi – Clarifo