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Financial Snapshot

Revenue
TTM
$0.00
Gross Margin
Last 4 Quarters
N/A
Net Income
TTM
-$13.13M
Current Assets
2026 Q1
Current Liabilities
2026 Q1
Current Ratio
2026 Q1
272.77%
Total Assets
2026 Q1
Total Liabilities
2026 Q1
Book Value
2026 Q1
9.073M
Cash
2026 Q1
P/E
Last 4 Quarters
N/A
Free Cash Flow
TTM
-$10.89M

Stock Price

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Market Cap: $13.995 Million

About MetaVia Inc

MetaVia Inc (NASDAQ: MTVA) is a clinical-stage biopharmaceutical company developing drug candidates for metabolic diseases including obesity, type 2 diabetes (T2DM), and metabolic dysfunction-associated steatohepatitis (MASH). The company generates no product revenue and funds operations through equity financing, including at-the-market offerings. As of December 31, 2025, MetaVia had $10.3 million in cash and cash equivalents, an accumulated deficit of $148.8 million, and incurred a net loss of $13.0 million (or $7.35 per basic and diluted share) for FY2025. The company has reported net losses and negative operating cash flows since inception and carries a going concern qualification, with net cash used in operating activities of $15.7 million for FY2025. Its pipeline includes Vanoglipel (DA-1241), a GPR119 agonist in Phase 2a for MASH and T2DM, and DA-1726, a GLP1R/GCGR dual agonist oxyntomodulin analog in Phase 1 for obesity. No products are approved or commercialized.

Revenue model
MetaVia has no approved products and generates no commercial revenue. Operations are funded through equity issuances, including at-the-market offerings and private placements. The company operates at a pre-revenue stage with all expenses directed toward clinical development.
Products and services
Vanoglipel (DA-1241): a GPR119 agonist in Phase 2a clinical development for MASH and T2DM, promoting release of GLP-1, GIP, and PYY gut peptides. DA-1726: a GLP1R and GCGR dual agonist oxyntomodulin analog in Phase 1 for obesity, designed for once-weekly subcutaneous administration. Phase 1 data presented at ObesityWeek 2025 (November 2025) showed favorable safety, tolerability, and reductions in body weight and waist circumference.
Customers and end markets
No commercial customers as of December 31, 2025. Target end markets are patients with obesity, type 2 diabetes, and MASH. Future customers, if products are approved, would include patients, physicians, hospitals, and third-party payors including Medicare and private insurers.
Value-chain role
Clinical-stage drug developer. MetaVia operates upstream in the pharmaceutical value chain, conducting preclinical and clinical trials. It has no manufacturing, commercialization, or distribution infrastructure disclosed in the filing.
Geographic exposure
Incorporated in Delaware and listed on Nasdaq. The filing references U.S. and European Union regulatory and pricing environments as relevant to future commercialization, but no geographic revenue breakdown exists given pre-revenue status.

Source: SEC 10-K, filed 2026-03-26

Industry: Pharmaceutical Preparations Peers: NeuBase Therapeutics, Inc. BIOCEPT INC Ernexa Therapeutics Inc Calithera Biosciences, Inc. Soleno Therapeutics Inc Cyclo Therapeutics, Inc. Transcode Therapeutics Inc

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