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WKN: A3C7A5 | ISIN: FR0012634822 | Ticker-Symbol: 4RD
Frankfurt
13.11.25 | 18:48
3,780 Euro
-0,26 % -0,010
Branche
Biotechnologie
Aktienmarkt
Sonstige
1-Jahres-Chart
MAAT PHARMA SA Chart 1 Jahr
5-Tage-Chart
MAAT PHARMA SA 5-Tage-Chart
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3,8103,93013.11.

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MAAT PHARMA Aktie jetzt für 0€ handeln
DoMaaT Pharma Launches a Capital Increase of Approximately €9 Million256Launch 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.MaaT Pharma Presents Updated Preclinical Data at SITC Annual Meeting Demonstrating Immune Activation and Anti-Tumor Activity of MaaT034272Regulatory 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.Original-Research: MaaT Pharma SACA (von First Berlin Equity Research GmbH): BUY203Original-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.MaaT Pharma Reports Financial Results for the Third Quarter 2025 and Provides Financing Update246The 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.MaaT Pharma's Xervyteg® shows 62% response rate in GI-aGvHD trial5
03.11.MaaT Pharma: Xervyteg® erzielt 62 % Ansprechrate in entscheidender Studie zu GI-aGvHD4
03.11.MaaT Pharma Announces Positive Phase 3 Results Evaluating Xervyteg (MaaT013) in Acute Graft-versus-Host Disease Selected for Oral Presentation at ASH Congress 2025237Oral 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.MaaT Pharma stock jumps 11% after DSMB clears Phase 2b trial to continue6
07.10.MaaT Pharma's MaaT033 For Allo-HSCT Patients Clears Second DSMB Safety Review In Phase 2b Trial2
07.10.MaaT Pharma Announces Positive Second Safety Interim Analysis from DSMB for Phase 2b PHOEBUS Trial Evaluating MaaT033 for Patients Receiving Allo-HSCT257The 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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17.09.MaaT Pharma Publishes Its Half Year 2025 Results and Provides a Business Update452Positive results from Phase 3 trial for MaaT013 in acute Graft-versus-Host disease (aGvHD); topline results showed a 62% gastrointestinal overall response rate at Day 28 and 1-year expected Overall...
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30.07.MaaT Pharma: €37.5 Million EIB Loan Secured To Advance Cancer Therapies3
28.07.MaaT Pharma Secures €37.5 Million Loan From European Investment Bank (EIB) Marking a New Step in Advancing its Clinical Program in Hemato-Oncology527Tranche-based financing to support clinical development for the Company's late-stage assets in hemato-oncology including Xervyteg currently under review for potential approval by the EMA and MaaT033...
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24.07.MaaT Pharma: Half-year Report to the Liquidity Contract With Kepler Cheuvreux291Regulatory 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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07.07.MaaT Pharma: Monthly Information Regarding the Total Number of Voting Rights and Shares Comprising the Share Capital303Article 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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02.07.MaaT Pharma Announces Exclusive Commercialization Partnership With Clinigen for Xervyteg in acute Graft-versus Host Disease in Europe514MaaT Pharma and Clinigen signed exclusive long-term licensing and distribution agreement and commercial supply agreement for Xervyteg(MaaT013), its first in class treatment proposed for patients...
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24.06.MaaT Pharma Presents the Results of its Annual Ordinary and Extraordinary General Meeting357Regulatory News: MaaT Pharma (EURONEXT: MAAT the "Company"), a clinical-stage biotechnology company and a leader in the development of Microbiome Ecosystem Therapies(MET) dedicated to enhancing...
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19.06.MaaT Pharma Provides a Business Update and Highlights Key Milestones Expected in 2025492Marketing Authorization application of Xervyteg (MaaT013) in acute graft-versus-host-disease submitted to the European Medicines Agency (EMA) in June 2025 MAA could be expected in H2 2026...
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13.06.MaaT Pharma Presents Updated Positive Data in Early Access Program for Xervyteg at the EHA Congress Validating High Efficacy Observed in Pivotal ARES Study in Acute Graft-versus-Host Disease439Oral presentation highlights updated data in Early Access Program (EAP) for 173 patients with acute Graft-vs-Host Disease (aGvHD) treated with Xervyteg Independent dataset from EAP reinforces...
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02.06.MaaT Pharma Advances Toward Commercialization And Submits Marketing Authorization Application to the European Medicines Agency (EMA) for Xervyteg (MaaT013) in Acute Graft-versus-Host Disease471MaaT Pharma submitted today a Marketing Authorization Application (MAA) to the European Medicines Agency (EMA) for its product candidate MaaT013, under the registered brand name of Xervyteg Xervyteghas...
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