MetaVia Receives Approval for DA-1726 Clinical Trial
Written by Emily J. Thompson, Senior Investment Analyst
Updated: Mar 18 2026
0mins
Should l Buy MTVA?
MetaVia announced that the Institutional Review Board, IRB, at Clinical Pharmacology of Miami has approved the Company's Phase 1 Part 3 clinical trial of its lead asset, DA-1726, a novel, dual oxyntomodulin analog targeting both GLP-1 and glucagon receptors. The approval enables initiation of Part 3 of the Phase 1 program, which consists of two 16-week titration cohorts evaluating one-step and two-step dose-escalation strategies intended to safely reach higher target doses and further optimize tolerability.
Trade with 70% Backtested Accuracy
Stop guessing "Should I Buy MTVA?" and start using high-conviction signals backed by rigorous historical data.
Sign up today to access powerful investing tools and make smarter, data-driven decisions.
Analyst Views on MTVA
Wall Street analysts forecast MTVA stock price to rise
2 Analyst Rating
2 Buy
0 Hold
0 Sell
Moderate Buy
Current: 1.170
Low
40.00
Averages
47.50
High
55.00
Current: 1.170
Low
40.00
Averages
47.50
High
55.00
About MTVA
MetaVia Inc. is a clinical-stage biotechnology company focused on transforming cardiometabolic diseases. It is developing DA-1726 for the treatment of obesity and is developing DA-1241 for the treatment of Metabolic Dysfunction-Associated Steatohepatitis (MASH). DA-1726 is a novel oxyntomodulin (OXM) analogue that functions as a glucagon-like peptide-1 receptor (GLP1R) and glucagon receptor (GCGR) dual agonist. OXM is a naturally occurring gut hormone that activates GLP1R and GCGR, thereby decreasing food intake while increasing energy expenditure, thus potentially resulting in superior body weight loss compared to selective GLP1R agonists. DA-1241 is a novel G-Protein-Coupled Receptor 119 (GPR119) agonist with development optionality as a standalone and/or combination therapy for both MASH and type 2 diabetes. Agonism of GPR119 in the gut promotes the release of key gut peptides, glucagon-like peptide 1, glucagon-dependent insulinotropic polypeptide receptor, and peptide YY.
About the author
Emily J. Thompson
Emily J. Thompson, a Chartered Financial Analyst (CFA) with 12 years in investment research, graduated with honors from the Wharton School. Specializing in industrial and technology stocks, she provides in-depth analysis for Intellectia’s earnings and market brief reports.
MetaVia Reports FY 2025 Financial Results with Significant Losses
- Financial Loss: MetaVia reported a GAAP EPS of -$7.35 for FY 2025, indicating significant challenges in profitability that could undermine investor confidence and future financing capabilities.
- Cash Position: As of December 31, 2025, MetaVia's cash and cash equivalents stood at $10.3 million, down from $16.0 million in 2024, highlighting increased liquidity pressure and the need for careful operational cash management.
- Funding Strategy: The company plans to bolster its finances through an $8.1 million underwritten public offering in January 2026, which is expected to improve cash flow and support operations into Q4 2026, ensuring continued market presence.
- Future Outlook: Despite the current financial difficulties, MetaVia aims to achieve long-term sustainability through new financing and operational efficiency improvements; however, ongoing losses may negatively impact its competitive position in the market.
See More
MetaVia Reports Phase 1 Data for DA-1726 Indicating Best-in-Class Potential
- Clinical Data Highlights: MetaVia's Phase 1 trial of DA-1726 at 48 mg demonstrated a 9.1% weight loss, significant improvements in glucose control, and direct liver benefits, indicating its best-in-class potential for treating obesity and related metabolic disorders.
- Improved Financial Position: The company raised $9.3 million through a public offering in January 2026, which is expected to fund the advancement of the DA-1726 program and sustain operations into the fourth quarter of 2026.
- Research Plan Update: With Institutional Review Board approval secured, the company plans to initiate a 16-week titration study for DA-1726 in April 2026, evaluating both 48 mg and 64 mg regimens, with data anticipated in the fourth quarter of 2026.
- Intellectual Property Protection: DA-1726 is supported by 39 granted and pending patents, ensuring protection in the U.S. and internationally at least through 2041, which further strengthens its competitive position in the market.
See More
MetaVia Unveils DA-1726 Phase 1 Data, Showcasing Best-in-Class Potential
- Clinical Data Highlights: MetaVia announced Phase 1 data for DA-1726 showing a 9.1% weight loss, significant improvements in glucose control, and liver health benefits, indicating its best-in-class potential for treating obesity and related metabolic disorders.
- Improved Financial Position: The company raised $9.3 million in a public offering in January 2026, expected to fund the advancement of the DA-1726 program and ensure operational cash flow through the fourth quarter of 2026.
- Intellectual Property Protection: MetaVia has established a robust intellectual property portfolio with 39 and 48 patents for DA-1726 and vanoglipel, respectively, ensuring competitive advantages in global markets with protection extending to 2041 and 2035.
- Future Clinical Plans: The company plans to initiate a Phase 1 Part 3, 16-week titration study for DA-1726 in April 2026, with data expected in the fourth quarter of 2026, further validating its efficacy in obesity treatment.
See More
META'S ANDY STONE RESPONDS TO LA VERDICT: WE DISAGREE AND PLAN TO APPEAL - X POST
- Meta's Response: Meta has expressed disagreement with the recent verdict and plans to appeal the decision.
- Legal Context: The statement indicates that Meta respects the legal process but does not agree with the outcome of the case.
See More
Life Sciences Virtual Investor Forum Highlights Available On-Demand
- Forum Overview: The Life Sciences Virtual Investor Forum, held on March 11-12, showcased innovative companies from biotechnology, medical devices, and pharmaceuticals, providing investors with insights into emerging technologies and strategic growth opportunities, thereby attracting significant investor interest.
- Presentation Access: Attendees can view forum presentations on-demand for 90 days, available 24/7, which enhances investor-company interaction and improves information transparency in the investment community.
- 1x1 Meeting Requests: Select companies are accepting management meeting requests through March 17, facilitating direct communication between investors and company executives, which strengthens investor relations management.
- Enhanced Investor Engagement: Virtual Investor Conferences provide a real-time interactive platform that allows companies to connect more efficiently with investors, significantly increasing investor engagement and marking an innovation in investor communication methods.
See More
MetaVia Announces Global Patent Portfolio Protecting Vanoglipel Until 2035
- Patent Portfolio Overview: MetaVia currently holds 48 granted and pending patents across the U.S., Europe, Japan, and China, ensuring intellectual property protection for its novel GPR119 agonist vanoglipel until 2035, demonstrating the company's robust R&D capabilities in cardiometabolic diseases.
- Licensing Advantage: The patent portfolio is exclusively licensed from Dong-A ST Co., Ltd., covering the core compound and manufacturing methods of vanoglipel, ensuring broad applicability in treating diseases linked to metabolic dysfunction, thereby enhancing MetaVia's market competitiveness.
- Clinical Trial Results: In multiple preclinical and Phase 1 and 2 clinical trials, vanoglipel has shown good tolerability and significant efficacy in treating Metabolic Dysfunction-Associated Steatohepatitis (MASH) and type 2 diabetes, further solidifying its market potential.
- Strategic Development Focus: CEO Hyung Heon Kim emphasized that maintaining and expanding intellectual property is central to the company's strategy to maximize the long-term value potential of vanoglipel, reflecting a strong commitment to innovative oral treatment solutions.
See More
MetaVia Reports FY 2025 Financial Results with Significant Losses
- Financial Loss: MetaVia reported a GAAP EPS of -$7.35 for FY 2025, indicating significant challenges in profitability that could undermine investor confidence and future financing capabilities.
- Cash Position: As of December 31, 2025, MetaVia's cash and cash equivalents stood at $10.3 million, down from $16.0 million in 2024, highlighting increased liquidity pressure and the need for careful operational cash management.
- Funding Strategy: The company plans to bolster its finances through an $8.1 million underwritten public offering in January 2026, which is expected to improve cash flow and support operations into Q4 2026, ensuring continued market presence.
- Future Outlook: Despite the current financial difficulties, MetaVia aims to achieve long-term sustainability through new financing and operational efficiency improvements; however, ongoing losses may negatively impact its competitive position in the market.
See More
MetaVia Reports Phase 1 Data for DA-1726 Indicating Best-in-Class Potential
- Clinical Data Highlights: MetaVia's Phase 1 trial of DA-1726 at 48 mg demonstrated a 9.1% weight loss, significant improvements in glucose control, and direct liver benefits, indicating its best-in-class potential for treating obesity and related metabolic disorders.
- Improved Financial Position: The company raised $9.3 million through a public offering in January 2026, which is expected to fund the advancement of the DA-1726 program and sustain operations into the fourth quarter of 2026.
- Research Plan Update: With Institutional Review Board approval secured, the company plans to initiate a 16-week titration study for DA-1726 in April 2026, evaluating both 48 mg and 64 mg regimens, with data anticipated in the fourth quarter of 2026.
- Intellectual Property Protection: DA-1726 is supported by 39 granted and pending patents, ensuring protection in the U.S. and internationally at least through 2041, which further strengthens its competitive position in the market.
See More
MetaVia Unveils DA-1726 Phase 1 Data, Showcasing Best-in-Class Potential
- Clinical Data Highlights: MetaVia announced Phase 1 data for DA-1726 showing a 9.1% weight loss, significant improvements in glucose control, and liver health benefits, indicating its best-in-class potential for treating obesity and related metabolic disorders.
- Improved Financial Position: The company raised $9.3 million in a public offering in January 2026, expected to fund the advancement of the DA-1726 program and ensure operational cash flow through the fourth quarter of 2026.
- Intellectual Property Protection: MetaVia has established a robust intellectual property portfolio with 39 and 48 patents for DA-1726 and vanoglipel, respectively, ensuring competitive advantages in global markets with protection extending to 2041 and 2035.
- Future Clinical Plans: The company plans to initiate a Phase 1 Part 3, 16-week titration study for DA-1726 in April 2026, with data expected in the fourth quarter of 2026, further validating its efficacy in obesity treatment.
See More
META'S ANDY STONE RESPONDS TO LA VERDICT: WE DISAGREE AND PLAN TO APPEAL - X POST
- Meta's Response: Meta has expressed disagreement with the recent verdict and plans to appeal the decision.
- Legal Context: The statement indicates that Meta respects the legal process but does not agree with the outcome of the case.
See More
Life Sciences Virtual Investor Forum Highlights Available On-Demand
- Forum Overview: The Life Sciences Virtual Investor Forum, held on March 11-12, showcased innovative companies from biotechnology, medical devices, and pharmaceuticals, providing investors with insights into emerging technologies and strategic growth opportunities, thereby attracting significant investor interest.
- Presentation Access: Attendees can view forum presentations on-demand for 90 days, available 24/7, which enhances investor-company interaction and improves information transparency in the investment community.
- 1x1 Meeting Requests: Select companies are accepting management meeting requests through March 17, facilitating direct communication between investors and company executives, which strengthens investor relations management.
- Enhanced Investor Engagement: Virtual Investor Conferences provide a real-time interactive platform that allows companies to connect more efficiently with investors, significantly increasing investor engagement and marking an innovation in investor communication methods.
See More
MetaVia Announces Global Patent Portfolio Protecting Vanoglipel Until 2035
- Patent Portfolio Overview: MetaVia currently holds 48 granted and pending patents across the U.S., Europe, Japan, and China, ensuring intellectual property protection for its novel GPR119 agonist vanoglipel until 2035, demonstrating the company's robust R&D capabilities in cardiometabolic diseases.
- Licensing Advantage: The patent portfolio is exclusively licensed from Dong-A ST Co., Ltd., covering the core compound and manufacturing methods of vanoglipel, ensuring broad applicability in treating diseases linked to metabolic dysfunction, thereby enhancing MetaVia's market competitiveness.
- Clinical Trial Results: In multiple preclinical and Phase 1 and 2 clinical trials, vanoglipel has shown good tolerability and significant efficacy in treating Metabolic Dysfunction-Associated Steatohepatitis (MASH) and type 2 diabetes, further solidifying its market potential.
- Strategic Development Focus: CEO Hyung Heon Kim emphasized that maintaining and expanding intellectual property is central to the company's strategy to maximize the long-term value potential of vanoglipel, reflecting a strong commitment to innovative oral treatment solutions.
See More
