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WKN: A41VBC | ISIN: US64132R5037 | Ticker-Symbol:
NASDAQ
12.12.25 | 21:58
9,380 US-Dollar
+9,58 % +0,820
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02.12.MetaVia announces 1-for-11 reverse stock split; shares slip over 15%4
02.12.MetaVia announces 1-for-11 reverse stock split effective December 43
02.12.MetaVia Inc. Announces 1-for-11 Reverse Stock Split106CAMBRIDGE, Mass., Dec. 2, 2025 /PRNewswire/ -- MetaVia Inc. (Nasdaq: MTVA) ("MetaVia" or the "Company"), a clinical-stage biotechnology company focused on transforming...
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26.11.MetaVia Inc. - 8-K, Current Report-
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 2025123Oral GPR119 Agonist Demonstrated Clinically Meaningful Reductions in HbA1c, Improvements in Liver Inflammation and Fibrosis, and Favorable Changes in Plasma Lipidomic...
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METAVIA Aktie jetzt für 0€ handeln
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 Update115Dosed 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 potential6
07.08.MetaVia Inc. - 10-Q, Quarterly Report4
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 Update139Dosed 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 Patient115Extension 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 Dose484Top-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
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