MetaVia CEO: DA-1726 Shows Significant Weight Loss Results
"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 analog agonist that functions as a glucagon-like peptide-1 receptor and glucagon receptor, for the treatment of obesity and related metabolic disorders," stated Hyung Heon Kim, CEO 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 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." Kim continued, "Beyond DA-1726, we continued to advance vanoglipel, a novel G-Protein-Coupled Receptor 119 agonist, with the presentation of positive Phase 2a data at the American Association for the Study of Liver Diseases The Liver Meeting 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 artificial intelligence 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."
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- Executive Forum Participation: MetaVia's CEO Hyung Heon Kim will participate in the Life Sciences Virtual Investor Forum on June 24, 2026, showcasing the company's innovative pipeline in obesity and metabolic therapies, which is expected to attract investor interest and enhance company visibility.
- Real-Time Interaction Opportunity: The forum will feature a live Q&A session, allowing investors to directly engage with the management team, thereby strengthening investor confidence in the company's future developments through enhanced interaction.
- New Drug Development Progress: MetaVia's DA-1726 has demonstrated best-in-class potential for weight loss in obesity treatment, showing promising results in clinical trials for glucose control and waist reduction, which could provide a significant competitive advantage in the market.
- Promising Drug Candidate: Vanoglipel, as a potential first-in-class drug, has shown direct hepatic action and metabolic improvement in clinical studies, and if successfully launched, it could open new revenue streams for the company and elevate its market position.
- Executive Forum Participation: MetaVia's CEO Hyung Heon Kim will participate in the Life Sciences Virtual Investor Forum on June 24, 2026, showcasing the company's innovative pipeline in obesity and metabolic therapies, which is expected to attract investor interest and enhance the company's visibility.
- Real-Time Interaction: The forum will feature a live Q&A session, allowing investors to directly engage with the management team, thereby strengthening investor confidence in the company's future prospects through enhanced interaction.
- New Drug Development Progress: MetaVia's DA-1726 has demonstrated best-in-class potential for weight loss in Phase 1 trials for obesity treatment, potentially outperforming existing GLP-1 receptor agonists, which could significantly enhance the company's competitive position in the biotechnology sector if successful.
- Potential First-in-Class Drug: Vanoglipel, targeting GPR119, has shown positive metabolic effects on glucose and lipid control in preclinical studies, and if validated in subsequent clinical trials, it could open new market opportunities for the company.
- Market Opportunities: Biotech companies are experiencing significant pre-market activity on Tuesday, driven by plans for market launches, acquisitions, financing deals, and AI training program launches, indicating potential investment opportunities.
- Notable Gains: Regentis Biomaterials Ltd. (RGNT) saw its stock price surge by 124% to $2.91, reflecting strong market confidence in its future growth and likely attracting more investor interest.
- Significant Losses: Park Ha Biological Technology Co., Ltd. (BYAH) experienced a 39% decline in its stock price to $1.61, indicating market concerns about its business outlook, which may lead investors to reassess their investment strategies.
- Increased Volatility: The price volatility among biotech stocks is heightened, particularly in the context of acquisitions and financing deals, prompting investors to closely monitor market dynamics to seize potential investment opportunities and risks.
- Clinical Trial Results: At the ADA 2026 conference, MetaVia presented that the 48 mg cohort of DA-1726 achieved up to 9.1% mean body weight reduction at Day 54 without evidence of plateau, indicating the drug's potential in obesity treatment and possibly enhancing future market acceptance.
- Safety and Tolerability: DA-1726 demonstrated good tolerability in the 48 mg cohort, with primarily mild-to-moderate gastrointestinal adverse events and no serious adverse events, laying a solid foundation for its further clinical development and boosting investor confidence.
- Combination Therapy Effects: The combination of vanoglipel with resmetirom showed a 23.6% weight reduction in mouse models, along with significant improvements in liver fat and inflammation markers, indicating its potential therapeutic value in metabolic diseases and possibly opening new market opportunities for MetaVia.
- Future Development Plans: MetaVia plans to release results from higher-dose DA-1726 clinical trials in Q4 2026, continuing to advance its research in obesity and metabolic diseases, demonstrating the company's long-term commitment and confidence in its product pipeline.
- Clinical Trial Results: At the ADA 2026 conference, MetaVia presented new Phase 1 results for DA-1726, achieving up to 9.1% weight loss at the 48 mg dose over 54 days without evidence of a plateau, indicating its potential in obesity treatment.
- Safety and Tolerability: DA-1726 demonstrated good tolerability in the 48 mg cohort, with primarily mild-to-moderate gastrointestinal adverse events and no serious adverse events, highlighting its safety profile for clinical use.
- Combination Therapy Effects: The combination of vanoglipel and resmetirom showed synergistic hepatoprotective and weight-loss effects in mouse models, achieving a 23.6% weight reduction and significantly improving liver fat and inflammation markers, supporting its potential in MASH treatment.
- Metabolic Improvements: When combined with metformin, vanoglipel reduced non-fasting glucose by 28.7% and body weight by 16.3%, demonstrating its advantages in type 2 diabetes treatment and further supporting its potential as a therapeutic combination strategy.
- Management Presentation: MetaVia Inc. will present updates on its novel obesity and metabolic therapies at the Emerging Growth Conference on June 11, 2026, at 3:25 PM ET, featuring insights from CEO Hyung Heon Kim and CFO Marshall H. Woodworth, showcasing the company's innovative advancements in cardiometabolic diseases.
- DA-1726 Clinical Trial: In a Phase 1 multiple ascending dose trial for obesity, DA-1726 demonstrated best-in-class potential for weight loss, glucose control, and waist reduction, functioning as a dual agonist for GLP-1 and GCGR, potentially outperforming selective GLP-1 receptor agonists like semaglutide in weight management.
- Positive Effects of Vanoglipel: As a novel GPR119 agonist, vanoglipel showed positive effects on liver inflammation, lipid metabolism, and glucose metabolism in preclinical studies, reducing hepatic steatosis, inflammation, and fibrosis, while also demonstrating direct hepatic action in a Phase 2a clinical study.
- Virtual Conference Logistics: Attendees can submit questions in advance, and a Q&A session will follow the presentation, while those unable to join live can access an archived webcast on MetaVia's events page, enhancing investor engagement and transparency.







