MetaVia's DA-1726 Shows Promising Weight Loss and Lipid Benefits—Key Phase 1 Results to Be Presented at ObesityWeek 2025


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MetaVia's DA-1726 Shows Promising Weight Loss and Lipid Benefits—Key Phase 1 Results to Be Presented at ObesityWeek 2025

Phase 1 Data Supports Once-Weekly Dosing and Early Efficacy for Obesity Treatment

MetaVia Inc. (NASDAQ: MTVA) is set to share new Phase 1 and pre-clinical data for its investigational obesity drug, DA-1726, at ObesityWeek 2025. The lead program is a novel, dual agonist targeting both the GLP-1 and glucagon receptors. According to MetaVia’s press release, DA-1726 has demonstrated a pharmacokinetic (PK) profile enabling convenient once-weekly dosing, as well as clinically meaningful reductions in weight and waist circumference—observed without the need for dose titration. Importantly, DA-1726 was well tolerated at all tested doses, and no serious adverse events or cardiovascular issues were observed.

Best-in-Class Weight and Lipid Results Distinguish DA-1726 from Peers

Results from the Phase 1 study show that, at the highest dose (32 mg), participants achieved an average weight loss of 4.3% over four weeks, with some losing as much as 6.3% from baseline. Waist circumference was reduced by up to 3.9 inches, and these benefits were maintained for two weeks after stopping the medication. Additionally, in pre-clinical obesity models, DA-1726 delivered lipid-lowering effects that outperformed competitors like pemvidutide and showed better weight loss than tirzepatide, even when subjects had similar food intake.

Feature DA-1726 Results Comparator Comparative Outcome
Average Weight Loss (Day 26) 4.3% Pemvidutide/Tirzepatide Comparable or Better
Maximum Weight Loss 6.3%
Waist Circumference Change -3.9 in
Lipid Lowering Superior (TC, LDL-C) Pemvidutide/Tirzepatide Superior
Dosing Once weekly Linear, dose-proportional
Half-Life ~80 hours Supports weekly regimen
Serious Adverse Events None reported

Safety and Convenience Drive Appeal in Obesity Market

DA-1726's safety profile stood out: gastrointestinal side effects were mild and short-lived, and the trial saw no participant dropouts or dose-limiting toxicities. Linear, dose-proportional PK and an approximately 80-hour half-life make it a strong candidate for convenient weekly dosing, reducing patient burden. Encouraged by these findings, MetaVia has extended its Phase 1 study to evaluate a higher, 48 mg dose for eight weeks, aiming for even greater long-term efficacy data.

Potential Competitive Edge in Obesity Drug Pipeline

What sets DA-1726 apart? Not only does it induce meaningful weight and waist reductions, but it also appears to improve lipid parameters more effectively than leading dual agonists. In mouse models, it drove more weight loss than tirzepatide with similar food intake, a signal of enhanced energy expenditure and potentially broader metabolic benefits. Unlike other options, DA-1726 also preserved lean mass and achieved improved lipid lowering compared to competitors—making it one to watch in the evolving landscape of obesity therapies.

Looking Ahead: Results from Higher Dose and Extended Studies Pending

Investors and researchers alike will be watching for results from the extended 48 mg cohort of the Phase 1 study later this year. As new data emerges from both the clinic and the lab, DA-1726’s profile as a potentially best-in-class dual agonist for obesity and related metabolic disorders is growing stronger. For those interested in deeper science or the competitive dynamics in obesity drug development, keeping an eye on MetaVia’s presentations at ObesityWeek 2025 could be insightful.


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