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WKN: A3C7A5 | ISIN: FR0012634822 | Ticker-Symbol: 4RD
Stuttgart
21.01.26 | 21:02
5,080 Euro
0,00 % 0,000
Branche
Biotechnologie
Aktienmarkt
Sonstige
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MAAT PHARMA SA Chart 1 Jahr
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5,0805,18021.01.

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MAAT PHARMA Aktie jetzt für 0€ handeln
DiMaaT Pharma startet Phase-2-Studie mit Mikrobiom-Therapie bei Lungenkrebs4
DiMaaT 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 Dysbiosis301IMMUNOLIFE, 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): BUY308Original-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-Studie5
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 Survival608Presentation 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): BUY277Original-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/RESUMPTION128FOLGENDE(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 Million422Regulatory 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/SUSPENSION253DAS/ 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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13.11.25MaaT Pharma Launches a Capital Increase of Approximately €9 Million527Launch of a Global Offering of new ordinary shares for approximately €9 million through a Private Placement aimed at qualified investors, and a PrimaryBid Offering aimed at retail investors via...
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05.11.25MaaT Pharma Presents Updated Preclinical Data at SITC Annual Meeting Demonstrating Immune Activation and Anti-Tumor Activity of MaaT034354Regulatory 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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04.11.25Original-Research: MaaT Pharma SACA (von First Berlin Equity Research GmbH): BUY268Original-Research: MaaT Pharma SACA - from First Berlin Equity Research GmbH 04.11.2025 / 11:37 CET/CEST Dissemination of a Research, transmitted by EQS News - a service of EQS Group. The issuer...
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04.11.25MaaT Pharma Reports Financial Results for the Third Quarter 2025 and Provides Financing Update327The Company received an upfront payment of €10.5 million in July 2025 after the signature of an exclusive license and distribution agreement with Clinigen. Subject to approval and grant of a Marketing...
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03.11.25MaaT Pharma's Xervyteg shows 62% response rate in GI-aGvHD trial5
03.11.25MaaT Pharma: Xervyteg erzielt 62 % Ansprechrate in entscheidender Studie zu GI-aGvHD4
03.11.25MaaT Pharma Announces Positive Phase 3 Results Evaluating Xervyteg (MaaT013) in Acute Graft-versus-Host Disease Selected for Oral Presentation at ASH Congress 2025336Oral presentation at ASH 2025 to feature pivotal Phase 3 results of Xervyteg (MaaT013), including previously disclosed primary endpoint data (62% GI-ORR at Day 28) and new findings on secondary...
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07.10.25MaaT Pharma stock jumps 11% after DSMB clears Phase 2b trial to continue6
07.10.25MaaT Pharma's MaaT033 For Allo-HSCT Patients Clears Second DSMB Safety Review In Phase 2b Trial2
07.10.25MaaT Pharma Announces Positive Second Safety Interim Analysis from DSMB for Phase 2b PHOEBUS Trial Evaluating MaaT033 for Patients Receiving Allo-HSCT336The DSMB conducted an unblinded safety review of data from the first 120 enrolled patients and identified no safety concerns and no excessive mortality related to MaaT033 as of today. The...
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