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MP

WKN: A3C7A5 | ISIN: FR0012634822 | Ticker-Symbol: 4RD
Stuttgart
29.10.26 | 21:55
1,042 Euro
0,00 % 0,000
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MAAT PHARMA SA Chart 1 Jahr
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19.10.MaaT Pharma Receives FDA Feedback Following Pre-IND Meeting Supporting Continued Development of MaaT034 in Solid Tumors398Positive pre-Investigational New Drug (pre-IND) interaction with the Food Drug Administration (FDA) on Chemistry, Manufacturing and Controls (CMC) and nonclinical topics supports MaaT034's continued...
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07.10.Original-Research: MaaT Pharma SACA (von First Berlin Equity Research GmbH): Under Review315Original-Research: MaaT Pharma SACA - from First Berlin Equity Research GmbH 07.10.2026 / 14:10 CET/CEST Dissemination of a Research, transmitted by EQS News - a service of EQS Group. The issuer...
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29.09.MaaT Pharma Publishes its Half-Year 2026 Results and Provides a Business Update562MaaT013 (Xervyteg): In September 2026, following the re-examination procedure, the CHMP maintained its negative opinion on the Conditional Marketing Authorization Application (MAA) for...
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21.09.MaaT Pharma Announces Upcoming Pre-IND Meeting with the FDA and Advances MaaT034 Toward Clinical Development in Solid Tumors517Pre-IND (Investigational New Drug) meeting with the U.S. Food and Drug Administration (FDA), focused on CMC (Chemistry, Manufacturing, and Controls), is scheduled for October 2026, representing...
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18.09.MaaT Pharma Provides Update on MaaT013 (Xervyteg) Potential Development Plan Following CHMP Negative Opinion After Re-examination645The Committee for Medicinal Products for Human Use (CHMP) of the European Medicines Agency (EMA) issued a negative opinion on the Company's application for a Conditional Marketing Authorization...
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15.09.MaaT Pharma Receives Negative CHMP Trend Vote for MaaT013 (Xervyteg) Following Re-Examination for its Conditional Marketing Authorization Application in Europe504MaaT Pharma was informed of a negative trend during the Committee for Medicinal Products for Human Use (CHMP)'s Oral Explanation meeting which took place on September 14, 2026 Formal CHMP...
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06.07.MaaT Pharma Presents the Results of its Annual General Meeting and Provides a Statement on its Half-Year Liquidity Contract424Regulatory 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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02.07.MaaT Pharma: Monthly Information Regarding the Total Number of Voting Rights and Shares Comprising the Share Capital495Article 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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30.06.Original-Research: MaaT Pharma SACA (von First Berlin Equity Research GmbH): Under review404Original-Research: MaaT Pharma SACA - from First Berlin Equity Research GmbH 30.06.2026 / 13:08 CET/CEST Dissemination of a Research, transmitted by EQS News - a service of EQS Group. The issuer...
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26.06.EMA committee issues negative opinion on MaaT Pharma's MaaT0135
26.06.MaaT Pharma Announces Plan to Request Re-Examination Following Negative CHMP Opinion for MaaT013 for the treatment of acute Graft-versus-Host Disease1.176The Committee for Medicinal Products for Human Use (CHMP) of the European Medicines Agency (EMA) issued a negative opinion on the conditional Marketing Authorization Application (MAA) for MaaT013...
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11.06.Original-Research: MaaT Pharma SACA (von First Berlin Equity Research GmbH): Under review349Original-Research: MaaT Pharma SACA - from First Berlin Equity Research GmbH 11.06.2026 / 13:07 CET/CEST Dissemination of a Research, transmitted by EQS News - a service of EQS Group. The issuer...
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26.05.MaaT Pharma Provides Business Update and Reports Financial Results for the First Quarter 20261.025MaaT013 (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 Disease1.002During 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, 2026463Regulatory 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): Buy404Original-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 Journal600CHRONOS 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 Updates748Potential 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 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 Transplantation528Regulatory 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 Management779Oral 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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