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WKN: A3C7A5 | ISIN: FR0012634822 | Ticker-Symbol: 4RD
Frankfurt
02.06.26 | 15:25
2,870 Euro
+0,35 % +0,010
Branche
Biotechnologie
Aktienmarkt
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MAAT PHARMA SA Chart 1 Jahr
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2,8402,88518:55

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26.05.MaaT Pharma Provides Business Update and Reports Financial Results for the First Quarter 2026568MaaT013 (Xervyteg): In May 2026, the Company was informed of a "negative trend" opinion on its Marketing Authorization Application from the Committee for Medicinal Products for Human Use...
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20.05.MaaT Pharma Provides an Update on the Application for Marketing Authorization of MaaT013 (Xervyteg) in the treatment of acute Graft-versus-Host Disease632During the Committee for Medicinal Products for Human Use (CHMP) of the European Medicines Agency (EMA) Oral Explanation, the Company received a "negative trend" opinion for the upcoming June...
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11.05.MaaT Pharma to Hold Annual General Meeting on June 16, 2026269Regulatory News: MaaT Pharma (EURONEXT: MAAT the "Company"), a clinical-stage biotechnology company and a leader in the development of Microbiome Ecosystem TherapiesTM (MET) dedicated to enhancing...
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21.04.Original-Research: MaaT Pharma SACA (von First Berlin Equity Research GmbH): Buy285Original-Research: MaaT Pharma SACA - from First Berlin Equity Research GmbH 21.04.2026 / 15:09 CET/CEST Dissemination of a Research, transmitted by EQS News - a service of EQS Group. The issuer...
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01.04.MaaT Pharma Announces Publication of Retrospective Data in Third-Line Acute GvHD from the CHRONOS Study in Bone Marrow Transplantation Journal397CHRONOS is one of the largest real-world studies including refractory GI-aGvHD patients (n=59) treated with third-line best available treatments other than microbiome-based therapy Results...
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31.03.MaaT Pharma Announces 2025 Annual Results and Provides Business Updates471Potential Pivotal Year for MaaT013 (Xervyteg): Marketing Authorization Application (MAA) in Europe for MaaT013 (Xervyteg) submitted to the European Medicines Agency (EMA) in June 2025 ...
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23.03.MaaT Pharma presents phase 3 trial results for aGvHD treatment2
23.03.MaaT Pharma Presents the ARES Phase 3 Pivotal Trial Final Data During the Presidential Plenary Session at the 52nd Annual Meeting of the European Society for Bone and Marrow Transplantation363Regulatory News: MaaT Pharma (EURONEXT: MAAT the "Company"), a clinical-stage biotechnology company and a leader in the development of Microbiome Ecosystem TherapiesTM (MET) dedicated to enhancing...
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09.03.MaaT Pharma to Present Four Abstracts at the 52nd European Bone Marrow Transplantation Annual Meeting and to Highlight Clinigen-Hosted Industry Symposium on acute GvHD Management567Oral presentation during Presidential Plenary Session to feature the final results of the ARES pivotal Phase 3 trial evaluating MaaT013 in acute Graft-versus-Host Disease (aGvHD) with gastrointestinal...
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03.02.MaaT Pharma: Monthly Information Regarding the Total Number of Voting Rights and Shares Comprising the Share Capital392Article 223-16 of the General Regulations of the Financial Markets Authority (AMF Autorité des Marchés Financiers) Regulatory News: MaaT Pharma (EURONEXT: MAAT the "Company"), a clinical-stage...
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20.01.MaaT Pharma startet Phase-2-Studie mit Mikrobiom-Therapie bei Lungenkrebs9
20.01.MaaT Pharma Announces First Patient Randomized in IMMUNOLIFE Phase 2 Study Sponsored by Gustave Roussy, To Explore the Role of the Gut Microbiome To Overcome ICI Resistance in Advanced NSCLC Patients with Antibiotic-Induced Dysbiosis646IMMUNOLIFE, a Phase 2 randomized exploratory study, will evaluate the potential of MaaT033 in combination with Cemiplimab versus Best Investigator Choice (i.e.: second line) in enhancing disease...
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10.12.25Original-Research: MaaT Pharma SACA (von First Berlin Equity Research GmbH): BUY459Original-Research: MaaT Pharma SACA - from First Berlin Equity Research GmbH 10.12.2025 / 11:25 CET/CEST Dissemination of a Research, transmitted by EQS News - a service of EQS Group. The issuer...
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08.12.25MaaT Pharma reports 54% one-year survival rate in pivotal GvHD trial4
08.12.25MaaT Pharma meldet 54 % Ein-Jahres-Überlebensrate in zulassungsrelevanter GvHD-Studie6
08.12.25MaaT Pharma Presents Pivotal ARES Phase 3 Results for MaaT013 (Xervyteg) in Acute GvHD at ASH 2025 Annual Congress and Announces 54% 1-Year Overall Survival778Presentation included previously disclosed primary results from the pivotal ARES Phase 3 single-arm trial evaluating MaaT013 (Xervyteg) in treating refractory severe acute Graft-versus-Host Disease...
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19.11.25Original-Research: MaaT Pharma SACA (von First Berlin Equity Research GmbH): BUY419Original-Research: MaaT Pharma SACA - from First Berlin Equity Research GmbH 19.11.2025 / 11:11 CET/CEST Dissemination of a Research, transmitted by EQS News - a service of EQS Group. The issuer...
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17.11.25XFRA 4RD: WIEDERAUFNAHME/RESUMPTION237FOLGENDE(S) INSTRUMENT(E) WIRD/ WERDEN WIEDER IN DEN HANDEL AUFGENOMMEN MIT FOLGENDEM TRADING SCHEDULE.THE FOLLOWING INSTRUMENT(S) IS/ARE RESUMED TRADING WITH FOLLOWING TRADING SCHEDULE:INSTRUMENT NAME...
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14.11.25MaaT Pharma Announces the Successful Completion of Its Global Offering of €9.1 Million554Regulatory News: THIS ANNOUNCEMENT AND THE INFORMATION CONTAINED HEREIN IS RESTRICTED AND IS NOT FOR RELEASE, PUBLICATION OR DISTRIBUTION, IN WHOLE OR IN PART, DIRECTLY OR INDIRECTLY, IN, INTO...
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14.11.25XFRA 4RD: AUSSETZUNG/SUSPENSION376DAS/ DIE FOLGENDE(N) INSTRUMENT(E) IST/ SIND AB SOFORT AUSGESETZT:THE FOLLOWING INSTRUMENT(S) IS/ ARE SUSPENDED WITH IMMEDIATE EFFECT:INSTRUMENT NAME KUERZEL/SHORTCODE ISIN BIS/UNTILMAAT PHARMA S.A....
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