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WKN: A3E2E8 | ISIN: US64132R4048 | Ticker-Symbol:
NASDAQ
19.11.25 | 21:43
0,771 US-Dollar
0,00 % 0,000
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Aktienmarkt
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07.11.Oraler GPR119-Agonist von MetaVia zeigt vielversprechende Wirkung bei MASH-Behandlung1
07.11.MetaVia Inc.: MetaVia Presents Positive New Phase 2a Data on Vanoglipel (DA-1241) in Patients with Presumed MASH at the AASLD The Liver Meeting 202598Oral GPR119 Agonist Demonstrated Clinically Meaningful Reductions in HbA1c, Improvements in Liver Inflammation and Fibrosis, and Favorable Changes in Plasma Lipidomic...
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06.11.MetaVia GAAP EPS of -$0.14 beats by $0.111
06.11.MetaVia Inc.: MetaVia Reports Third Quarter 2025 Financial Results and Provides Corporate Update80Dosed the First Patient in the 8-Week 48 mg MAD Cohort of its Phase 1 Clinical Trial to Further Explore Non-Titrated Maximum Tolerated Dose of DA-1726 for the Treatment...
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06.11.MetaVia Inc. - 8-K, Current Report-
04.11.MetaVia's obesity drug shows promising weight loss in early trials1
04.09.H.C. Wainwright initiates MetaVia stock with Buy rating on metabolic drug potential5
07.08.MetaVia Inc. - 10-Q, Quarterly Report4
METAVIA Aktie jetzt für 0€ handeln
07.08.MetaVia GAAP EPS of -$0.26 misses by $0.041
07.08.MetaVia Inc.: MetaVia Reports Second Quarter 2025 Financial Results and Provides Corporate Update119Dosed the First Patient in the 8-Week 48 mg MAD Cohort of its Phase 1 Clinical Trial to Further Explore Maximum Tolerated Dose of DA-1726 for the Treatment of Obesity...
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06.08.MetaVia Inc.: MetaVia Extends 48 mg MAD Portion of Its Phase 1 Clinical Trial of DA-1726 for the Treatment of Obesity to 8 Weeks and Announces Fifth Weekly Dose in First Patient100Extension is Designed to Assess Early Efficacy and Patient Safety and Tolerability with Longer-Term Exposure to DA-1726 and Further Explore Non-Titrated Maximum...
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04.08.MetaVia Inc. - 8-K, Current Report1
09.07.MetaVia Inc. - 8-K, Current Report1
09.07.MetaVia Inc.: MetaVia Doses First Patient in the 48 mg MAD Cohort of Its Phase 1 Clinical Trial Evaluating DA-1726 for the Treatment of Obesity to Further Explore Maximum Tolerated Dose464Top-Line Data Expected in the Fourth Quarter of 2025 CAMBRIDGE, Mass., July 9, 2025 /PRNewswire/ -- MetaVia Inc. (Nasdaq: MTVA), a clinical-stage biotechnology...
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02.07.MetaVia registers 14.1M shares for resale1
30.06.MetaVia Inc. - 8-K, Current Report3
30.05.MetaVia Inc. erhält Mitteilung über Nichteinhaltung der Nasdaq-Vorschriften2
30.05.MetaVia Inc. - 8-K, Current Report2
14.05.MetaVia Inc.: MetaVia Reports First Quarter 2025 Financial Results and Provides Corporate Update428Announced Positive Top-Line Phase 1 MAD Trial Results for DA-1726 in Obesity, Demonstrating Compelling Weight Loss and Best-in-Class Potential for Glucose Control...
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22.04.MetaVia Inc.: MetaVia Reports Additional Positive Top-Line Results From the MAD Part 2 of Its Phase 1 Study of DA-1726, a Novel 3:1 Ratio GLP-1 and Glucagon Dual Receptor Agonist to Treat Obesity, Further Demonstrating Its ...154A Dose-Dependent Response in Body Weight Reduction Was Observed Between 8 mg and 32 mg DosesChange in BMI and Body Weight Adjusted for Height In the Treatment Groups, Showed a Significant...
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