Press Release: MetaVia Reports Year End 2025 Financial Results and Provides Corporate Update

Dow Jones03-26 20:31

48 mg Phase 1 Data Demonstrate Potential Best-in-Class Profile for DA-1726 with 9.1% Weight Loss, Improved Glucose Control and Direct Liver Benefit

Planned Phase 1 Part 3 16-Week Titration Study to Evaluate 48 mg (1-Step) and 64 mg (2-Step) Regimen Receives IRB Approval; Initiation Expected in April of 2026 with Data Anticipated in the Fourth Quarter

$10.3 Million in Cash and Cash Equivalents at End of Year and Proceeds From January 2026 Public Offering is Expected to Fund the Company Into the Fourth Quarter of 2026

CAMBRIDGE, Mass., March 26, 2026 /PRNewswire/ -- MetaVia Inc. (Nasdaq: MTVA), a clinical-stage biotechnology company focused on transforming cardiometabolic diseases, today announced financial results for the year ended December 31, 2025, and provided a corporate strategic update.

"We made significant progress advancing our cardiometabolic portfolio during the year, punctuated by the positive data, released in January of this year, from the Phase 1 extended 8-week, non-titrated 48 mg cohort of lead asset DA-1726, a novel, dual oxyntomodulin $(OXM)$ analog agonist that functions as a glucagon-like peptide-1 receptor (GLP1R) and glucagon receptor (GCGR), for the treatment of obesity and related metabolic disorders," stated Hyung Heon Kim, Chief Executive Officer of MetaVia. "These results demonstrated robust early weight loss, statistically significant reductions in waist circumference, strong improvements in glucose control, and meaningful reductions in liver stiffness, all achieved without titration and with a favorable safety and tolerability profile. We believe this combination of weight loss, glycemic control, direct hepatic benefit and tolerability meaningfully differentiates DA-1726 and supports its potential to deliver a best-in-class profile in obesity and broader cardiometabolic disease. Importantly, DA-1726 is supported by a growing intellectual property estate comprising 39 granted and pending patents in the United States and internationally, providing protection at least through 2041."

"On the heels of the positive Phase 1 data, we strengthened our balance sheet in January with gross proceeds of $9.3 million from an underwritten public offering, providing additional capital to advance the DA-1726 program. Having recently received Institutional Review Board (IRB) approval from the Clinical Pharmacology of Miami, we expect to initiate dosing in our Phase 1 Part 3, 16-week titration studies evaluating escalation to 48 mg in a single step and 64 mg using a two-step regimen in April, with data anticipated in the fourth quarter of 2026."

Mr. Kim continued, "Beyond DA-1726, we continued to advance vanoglipel (DA-1241), a novel G-Protein-Coupled Receptor 119 (GPR119) agonist, with the presentation of positive Phase 2a data at the American Association for the Study of Liver Diseases (AASLD) The Liver Meeting$(R)$ 2025, highlighting clinically meaningful improvements in glucose control, liver health and plasma lipidomic profiles over 16 weeks. In parallel, results from our collaboration with Syntekabio using the DeepMatcher(R) artificial intelligence (AI) platform confirmed strong inflammatory and cardiometabolic target engagement, further supporting development of vanoglipel in MASH and, potentially, in type 2 diabetes. We believe both programs position MetaVia at the forefront of next-generation cardiometabolic innovation as we move into 2026."

Fourth Quarter 2025 and Subsequent Highlights

   -- March 2026: Received IRB approval from Clinical Pharmacology of Miami for 
      the Phase 1 Part 3 16-week titration study of DA-1726, enabling 
      higher-dose evaluation in obese, otherwise healthy adults. 
 
   -- March 2026: Announced a comprehensive global intellectual property 
      portfolio supporting vanoglipel with 48 granted and pending patents 
      across three patent families in the U.S., Europe, Japan, China and other 
      countries, providing protection into 2035, unless extended further. 
      Exclusively licensed from Dong-A ST Co., Ltd., the patent portfolio 
      provides broad protection for vanoglipel itself, how it is manufactured, 
      and its potential use across a range of serious metabolic and liver 
      conditions. 
 
   -- February 2026: Strengthened global intellectual property position for 
      DA-1726 with 39 granted and pending patents in the U.S. and 
      internationally, providing protection through at least 2041, unless 
      extended further. Exclusively licensed from Dong-A ST Co., Ltd., the 
      portfolio broadly covers DA-1726's novel peptide structure, its 
      long-acting dual-incretin design, and therapeutic use across obesity, 
      metabolic disease, and related cardiometabolic conditions. 
 
   -- February 2026: Announced positive AI-modeling results from the ongoing 
      collaboration with Syntekabio, Inc., an AI-driven drug discovery company, 
      leveraging their proprietary DeepMatcher(R) platform. The results 
      confirmed vanoglipel's strong inflammatory and cardiometabolic target 
      engagement, supporting development in MASH and, potentially, type 2 
      diabetes. 
 
   -- January 2026: Closed an underwritten public offering of shares of common 
      stock, pre-funded warrants, Series C Common Warrants and Series D Common 
      Warrants for gross proceeds of approximately $9.3 million, prior to 
      deducting underwriting discounts and commissions and offering expenses 
      and excluding any potential future proceeds from the exercise of 
      warrants. 
 
   -- January 2026: Announced positive statistically significant results from 
      the 8-week (extended from four weeks) non-titrated 48 mg MAD cohort of 
      the Phase 1 clinical trial of DA-1726. The results showed robust early 
      weight loss, statistically significant reductions in waist circumference, 
      strong improvements in glucose control, and meaningful reductions in 
      liver stiffness, alongside a favorable safety and tolerability profile. 
 
   -- November 2025: Presented positive new data from the Phase 2a clinical 
      trial evaluating vanoglipel as a potential treatment for MASH in a poster 
      presentation at the AASLD The Liver Meeting(R) 2025. The data highlight 
      vanoglipel's differentiated dual activity across both hepatic and 
      metabolic pathways, demonstrating clinically meaningful improvements in 
      glucose control, liver health, and plasma lipidomic profiles following 16 
      weeks of treatment. 
 
   -- November 2025: Presented new Phase 1 and pre-clinical data on DA-1726 in 
      two poster presentations at ObesityWeek(R) 2025. The Phase 1 data 
      demonstrated favorable safety and tolerability, a newly characterized 
      pharmacokinetic $(PK)$ profile supporting once-weekly dosing, and 
      meaningful reductions in body weight and waist circumference following 
      four weeks of treatment. Additionally, in a diet-induced obesity (DIO) 
      mouse model, DA-1726 achieved comparable weight loss to pemvidutide with 
      superior lipid-lowering efficacy. 

Anticipated Clinical Milestones

   -- DA-1726 in Obesity: 
 
          -- Dosing of the first patient in the company's Phase 1 Part 3, 
             16-week titration studies, evaluating titration to 48 mg in one 
             step and 64 mg via a two-step regimen, is expected in April of 
             2026. 
 
          -- Data readout for these Phase 1 studies is expected in the fourth 
             quarter of 2026. 
 
   -- Vanoglipel (DA-1241) in MASH: 
 
          -- The Company is currently working to schedule an end-of-Phase 2 
             meeting with the FDA. 

Fourth Quarter Financial and Operating Results

   -- Research and Development (R&D) Expenses were approximately $6.8 million 
      for the year ended December 31, 2025, as compared to approximately $21.6 
      million for the year ended December 31, 2024. The decrease of 
      approximately $14.8 million was primarily attributable to (i) $10.8 
      million in lower direct R&D expenses related to vanoglipel (DA-1241) 
      product development, (ii) $3.9 million in lower direct R&D expenses 
      related to DA-1726 product development, and (iii) $0.2 million in lower 
      direct other R&D costs. These decreases were partially offset by $0.1 
      million in higher indirect consulting expenses and a slight increase in 
      indirect employee compensation and benefits. Included in direct R&D costs 
      were expenses totaling $3.4 million and $4.9 million for 2025 and 2024, 
      respectively, related to investigational drug manufacturing, non-clinical 
      and preclinical costs incurred under the Shared Services Agreement with 
      Dong-A ST (related party). 
   -- General and Administrative (G&A) Expenses were approximately $6.9 million 
      for the year ended December 31, 2025, as compared to approximately $7.3 
      million for the year ended December 31, 2024. The approximately $0.4 
      million decrease was primarily attributable to (i) $0.7 million in lower 
      consulting expenditures, (ii) $0.1 million in lower insurance, and (iii) 
      $0.2 million in lower other G&A expenses. These decreases were partially 
      offset by $0.5 million in higher legal and professional fees and $0.1 
      million in higher employee compensation and benefits. 
   -- Total Operating Expenses were approximately $13.7 million for the year 
      ended December 31, 2025, compared to approximately $28.8 million for the 
      year ended December 31, 2024. The approximately $15.1 million decrease 
      was primarily attributable to lower R&D expenses and G&A expenses. 
   -- Total Other Income was approximately $0.7 million for the year ended 
      December 31, 2025, compared to approximately $1.2 million for the year 
      ended December 31, 2024. The approximately $0.5 million decrease was 
      primarily attributable to (i) $0.4 million in lower interest income, net, 
      due to lower cash balances and lower interest rates, and (ii) $0.1 

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March 26, 2026 08:31 ET (12:31 GMT)

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