MetaVia Regains Compliance with Nasdaq Minimum Bid Price Requirement
MetaVia (Nasdaq: MTVA) announced on December 22, 2025 that it received Nasdaq notice dated December 19, 2025 confirming the company has regained compliance with Nasdaq's minimum bid price requirement under Listing Rule 5550(a)(2).
Rhea-AI Summary
MetaVia (Nasdaq: MTVA) announced on December 22, 2025 that it received Nasdaq notice dated December 19, 2025 confirming the company has regained compliance with Nasdaq's minimum bid price requirement under Listing Rule 5550(a)(2).
The notice states MetaVia also satisfies all other applicable Nasdaq listing criteria and that the related listing matter has been closed on the Nasdaq Capital Market.
Positive
- Regained Nasdaq compliance with minimum bid price on Dec 19, 2025
- Listing matter formally closed by Nasdaq for continued Nasdaq Capital Market listing
Negative
- None.
Details
News Market Reaction – MTVA
In the Dec 22 session, MTVA gained 11.60%, reflecting a significant positive market reaction.
Data tracked by StockTitan Argus on the day of publication.
Key Figures
- Nasdaq notice date
- December 19, 2025
- Date Nasdaq confirmed MetaVia regained minimum bid price compliance
- Listing rule
- Rule 5550(a)(2)
- Nasdaq minimum bid price requirement referenced in the notice
Historical Context
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1-for-11 reverse split aimed at meeting Nasdaq listing requirements.
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Positive Phase 2a vanoglipel data in presumed MASH at AASLD 2025.
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Q3 2025 results and pipeline update including DA-1726 and vanoglipel.
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Phase 1 and preclinical DA-1726 data presented at ObesityWeek 2025.
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Announcement of vanoglipel poster presentation at AASLD Liver Meeting.
24h Move is the share-price change in the day after each event; other market factors may also have contributed.
Key Terms
nasdaq's minimum bid price requirement regulatory
the nasdaq capital market regulatory
AI-generated analysis. How Rhea-AI works. Not financial advice.
About MetaVia
MetaVia Inc. is a clinical-stage biotechnology company focused on transforming cardiometabolic diseases. The company is currently developing DA-1726 for the treatment of obesity, and is developing vanoglipel (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. In a Phase 1 multiple ascending dose (MAD) trial in obesity, DA-1726 demonstrated best-in-class potential for weight loss, glucose control, and waist reduction. Vanoglipel is a novel G-protein-coupled receptor 119 (GPR119) agonist that promotes the release of key gut peptides GLP-1, GIP, and PYY. In pre-clinical studies, vanoglipel demonstrated a positive effect on liver inflammation, lipid metabolism, weight loss, and glucose metabolism, reducing hepatic steatosis, hepatic inflammation, and liver fibrosis, while also improving glucose control. In a Phase 2a clinical study, vanoglipel demonstrated direct hepatic action in addition to its glucose lowering effects.
For more information, please visit www.metaviatx.com.
Contacts:
MetaVia
Marshall H. Woodworth
Interim Chief Financial Officer
+1-857-299-1033
marshall.woodworth@metaviatx.com
Rx Communications Group
Michael Miller
+1-917-633-6086
mmiller@rxir.com
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SOURCE MetaVia Inc.
FAQ
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