Articles from MaaT Pharma

MaaT Pharma Announces Publication of Retrospective Data in Third-Line Acute GvHD from the CHRONOS Study in Bone Marrow Transplantation Journal
Regulatory News:
By MaaT Pharma · Via Business Wire · April 1, 2026
MaaT Pharma Announces 2025 Annual Results and Provides Business Updates
Regulatory News:
By MaaT Pharma · Via Business Wire · March 31, 2026
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 Transplantation
Regulatory News:
By MaaT Pharma · Via Business Wire · March 23, 2026
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 Management
Regulatory News:
By MaaT Pharma · Via Business Wire · March 9, 2026
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 Dysbiosis
Regulatory News:
By MaaT Pharma · Via Business Wire · January 20, 2026
MaaT Pharma Presents Pivotal ARES Phase 3 Results for MaaT013 (Xervyteg®) in Acute GvHD at ASH 2025 Annual Congress and Announces 54% 1-Year Overall Survival
Regulatory News:
By MaaT Pharma · Via Business Wire · December 8, 2025
MaaT Pharma Presents Updated Preclinical Data at SITC Annual Meeting Demonstrating Immune Activation and Anti-Tumor Activity of MaaT034
Regulatory News:
By MaaT Pharma · Via Business Wire · November 5, 2025
MaaT Pharma Reports Financial Results for the Third Quarter 2025 and Provides Financing Update
Regulatory News:
By MaaT Pharma · Via Business Wire · November 4, 2025
MaaT Pharma Announces Positive Phase 3 Results Evaluating Xervyteg® (MaaT013) in Acute Graft-versus-Host Disease Selected for Oral Presentation at ASH Congress 2025
Regulatory News:
By MaaT Pharma · Via Business Wire · November 3, 2025
MaaT Pharma Announces Positive Second Safety Interim Analysis from DSMB for Phase 2b PHOEBUS Trial Evaluating MaaT033 for Patients Receiving Allo-HSCT
Regulatory News:
By MaaT Pharma · Via Business Wire · October 7, 2025
MaaT Pharma Publishes Its Half Year 2025 Results and Provides a Business Update
Regulatory News:
By MaaT Pharma · Via Business Wire · September 17, 2025
MaaT Pharma Secures €37.5 Million Loan From European Investment Bank (EIB) Marking a New Step in Advancing its Clinical Program in Hemato-Oncology
Regulatory News:
By MaaT Pharma · Via Business Wire · July 28, 2025
MaaT Pharma Announces Exclusive Commercialization Partnership With Clinigen for Xervyteg® in acute Graft-versus Host Disease in Europe
Regulatory News:
By MaaT Pharma · Via Business Wire · July 2, 2025
MaaT Pharma Provides a Business Update and Highlights Key Milestones Expected in 2025
Regulatory News:
By MaaT Pharma · Via Business Wire · June 19, 2025
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 Disease
Regulatory News:
By MaaT Pharma · Via Business Wire · June 13, 2025
MaaT Pharma Advances Toward Commercialization And Submits Marketing Authorization Application to the European Medicines Agency (EMA) for Xervyteg® (MaaT013) in Acute Graft-versus-Host Disease
Regulatory News:
By MaaT Pharma · Via Business Wire · June 2, 2025
MaaT Pharma To Present Updated Data for MaaT013 in Early Access Program at the European Hematology Association (EHA) Annual Congress
Regulatory News:
By MaaT Pharma · Via Business Wire · May 14, 2025
MaaT Pharma Provides Business Update and Reports Financial Results for the First Quarter 2025
Regulatory News:
By MaaT Pharma · Via Business Wire · May 13, 2025
MaaT Pharma Announces Promising Final Data Readout for Phase 1b Evaluating MaaT033 in Amyotrophic Lateral Sclerosis (ALS)
Regulatory News:
By MaaT Pharma · Via Business Wire · May 12, 2025
MaaT Pharma Presents Preclinical Data at AACR Annual Meeting Demonstrating Immune Activation and Anti-Tumor Activity of MaaT034
Regulatory News:
By MaaT Pharma · Via Business Wire · April 28, 2025
MaaT Pharma Announces Positive Safety Interim Analysis from DSMB for Phase 2b Trial Evaluating MaaT033 for Patients Receiving Allo-HSCT
Regulatory News:
By MaaT Pharma · Via Business Wire · April 8, 2025
MaaT Pharma Announces Initiation of Coverage of its Stock by H.C. Wainwright & Co
Regulatory News:
By MaaT Pharma · Via Business Wire · April 7, 2025
MaaT Pharma: Monthly Information Regarding the Total Number of Voting Rights and Shares Comprising the Share Capital
Regulatory News:
By MaaT Pharma · Via Business Wire · April 4, 2025
MaaT Pharma To Present New Promising Preclinical Data at AACR for MaaT034 Aiming To Improve Patients’ Responses to Immunotherapies
Regulatory News:
By MaaT Pharma · Via Business Wire · March 31, 2025
MaaT Pharma Completes a Capital Increase of €13 Million with Historical Shareholders and Announces 2024 Annual Results
Regulatory News:
By MaaT Pharma · Via Business Wire · March 27, 2025
MaaT Pharma Announces Positive Outcomes from Final DSMB Meeting for Pivotal Phase 3 Clinical Trial Evaluating MaaT013 in Acute Graft-versus-Host Disease
Regulatory News:
By MaaT Pharma · Via Business Wire · March 18, 2025
MaaT Pharma Receives Positive Opinion from EMA Pediatric Committee on the Pediatric Investigation Plan for MaaT013
Regulatory News:
By MaaT Pharma · Via Business Wire · March 11, 2025
MaaT Pharma Announces Positive Second DSMB Review of Ongoing Phase 2b Clinical Trial Evaluating MaaT033 for Patients Receiving Allo-HSCT
Regulatory News:
By MaaT Pharma · Via Business Wire · January 21, 2025
MaaT Pharma Announces Positive Topline Results from the Pivotal Phase 3 ARES Study Evaluating MaaT013 in acute Graft-versus-Host Disease
Regulatory News:
By MaaT Pharma · Via Business Wire · January 8, 2025
CORRECTING and REPLACING: MaaT Pharma Presented Positive Updated Data on MaaT013 in the Early Access Program at ASH 2024 Annual Meeting
Regulatory News:
By MaaT Pharma · Via Business Wire · December 9, 2024
MaaT Pharma Presented Positive Updated Data on MaaT013 in the Early Access Program at ASH 2024 Annual Meeting
Regulatory News:
By MaaT Pharma · Via Business Wire · December 9, 2024
MaaT Pharma Announces First U.S. Patient Treated at City of Hope Under Single Patient Expanded Access for MaaT013 in Acute Graft-versus-Host Disease
Regulatory News:
By MaaT Pharma · Via Business Wire · December 5, 2024
MaaT Pharma Announces Positive Phase 1b Results, Meeting Primary Endpoint in the Evaluation of MaaT033 in Amyotrophic Lateral Sclerosis (ALS)
Regulatory News:
By MaaT Pharma · Via Business Wire · November 26, 2024
MaaT Pharma to Present Updates from Early Access Program at the 2024 ASH Annual Meeting Demonstrating Prolonged Long-Term Survival in Patients Receiving MaaT013 in aGvHD
Regulatory News:
By MaaT Pharma · Via Business Wire · November 7, 2024
MaaT Pharma Provides Third Quarter 2024 Business and Financial Results and Announces Management Changes
Regulatory News:
By MaaT Pharma · Via Business Wire · November 5, 2024
MaaT Pharma Completes Recruitment of its ARES Phase 3 Trial for MaaT013 to Treat Acute Graft-versus-Host Disease
Regulatory News:
By MaaT Pharma · Via Business Wire · October 15, 2024
MaaT Pharma Publishes its Half Year 2024 Results and Provides a Business Update
Regulatory News:
By MaaT Pharma · Via Business Wire · September 19, 2024
MaaT Pharma To Present and Participate in Investor and Medical Conferences in September
Regulatory News:
By MaaT Pharma · Via Business Wire · September 4, 2024
MaaT Pharma Announces First DSMB Positive Review of Ongoing Phase 2 Clinical Trial Evaluating MaaT033 for Patients Receiving Allo-HSCT
Regulatory News:
By MaaT Pharma · Via Business Wire · July 2, 2024
MaaT Pharma Announces Initiation of Coverage of its Stock by Stifel with a Buy Rating and a Target Price of EUR 16
Regulatory News:
By MaaT Pharma · Via Business Wire · June 25, 2024
MaaT Pharma Appoints Gianfranco Pittari, M.D. Ph.D, as Chief Medical Officer
Regulatory News:
By MaaT Pharma · Via Business Wire · June 24, 2024
MaaT Pharma Provides a Business Update and Highlights Key Milestones Expected in 2024
Regulatory News:
By MaaT Pharma · Via Business Wire · May 7, 2024
MaaT Pharma Presents Positive 18-month Data for MaaT013 Showing a Clear Overall Survival Advantage in aGvHD from the Early Access Program at the 2024 EBMT Event
Regulatory News:
By MaaT Pharma · Via Business Wire · April 15, 2024
MaaT Pharma Presents Promising Preclinical Data at AACR for MaaT034 Aiming To Improve Patients’ Responses to Immunotherapies
Regulatory News:
By MaaT Pharma · Via Business Wire · April 8, 2024
MaaT Pharma Announces Initiation of Coverage of its Stock by Gilbert Dupont/ Groupe Société Générale
Regulatory News:
By MaaT Pharma · Via Business Wire · April 5, 2024
MaaT Pharma Announces 2023 Annual Results and Provides a Business Overview
Regulatory News:
By MaaT Pharma · Via Business Wire · March 28, 2024
MaaT Pharma Strengthens Executive Team Appointing Jonathan Chriqui as Chief Business Officer
Regulatory News:
By MaaT Pharma · Via Business Wire · March 21, 2024
MaaT Pharma To Present New Preclinical Data at AACR for MaaT034 Aiming To improve Patients’ Responses to Immunotherapies
Regulatory News:
By MaaT Pharma · Via Business Wire · March 19, 2024
MaaT Pharma Announces Long Term Follow-Up Data for MaaT013 in Early Access Program to be Presented at the Upcoming EBMT Conference
Regulatory News:
By MaaT Pharma · Via Business Wire · March 12, 2024
MaaT Pharma indicates completion of Patient Recruitment for the Phase 2a Investigator-Sponsored Randomized Clinical Trial Evaluating MaaT013 in Combination with Immune Checkpoint Inhibitors in Metastatic Melanoma
Regulatory News:
By MaaT Pharma · Via Business Wire · March 5, 2024
MaaT Pharma Announces Positive Review from the DSMB on the Ongoing Phase 1 Clinical Trial Evaluating MaaT033 in Amyotrophic Lateral Sclerosis (ALS)
Regulatory News:
By MaaT Pharma · Via Business Wire · February 29, 2024
MaaT Pharma to Host Virtual KOL Event on MaaT013 and MaaT033 Following ASH 2023 Presentations
Regulatory News:
By MaaT Pharma · Via Business Wire · December 12, 2023
MaaT Pharma Presents Positive Results with Lead Product MaaT013 and Provides Insights on Ongoing Phase 2b Trial with MaaT033 at ASH 2023
Regulatory News:
By MaaT Pharma · Via Business Wire · December 11, 2023
MaaT Pharma, Leader in Development of Microbiome-Based Therapies in Oncology, Awarded Government Funding for Clinical Development of MaaT033 as part of the France 2030 Plan
Regulatory News:
By MaaT Pharma · Via Business Wire · November 30, 2023
MaaT Pharma Provides Third Quarter 2023 Business Update and Reports Financial Results
Regulatory News:
By MaaT Pharma · Via Business Wire · November 9, 2023
MaaT Pharma Announces First Patient Dosed in Phase 2b Randomized Clinical Trial Evaluating MaaT033 in Patients Receiving Allo-HSCT
Regulatory News:
By MaaT Pharma · Via Business Wire · November 6, 2023
MaaT Pharma Announces Two Poster Presentations for MaaT013 and MaaT033 at the Upcoming ASH Conference
Regulatory News:
By MaaT Pharma · Via Business Wire · November 2, 2023
MaaT Pharma to Present Preclinical Data at SITC on MaaT034, an Artificial Intelligence-Generated Product Aimed at Improving Patients’ Responses to Immunotherapies
Regulatory News:
By MaaT Pharma · Via Business Wire · October 31, 2023
MaaT Pharma Announces Positive Outcome Following DSMB Review Reinforcing Confidence in Phase 3 On-Going Trial in Acute Graft-versus-Host Disease with MaaT013
Regulatory News:
By MaaT Pharma · Via Business Wire · October 26, 2023
MaaT Pharma Publishes its Half Year 2023 Results and Provides a Business Update
Regulatory News:
By MaaT Pharma · Via Business Wire · September 26, 2023
MaaT Pharma and Skyepharma Complete Construction of Europe’s Largest Manufacturing Facility for Microbiome Ecosystem Therapies
MaaT Pharma (EURONEXT: MAAT – the “Company”), a clinical-stage biotech company and a leader in the development of Microbiome Ecosystem TherapiesTM (MET) dedicated to improving survival outcomes for patients with cancer, and Skyepharma, a French independent CDMO, expert in providing innovative solutions for bioproduction as well as complex drugs development and manufacturing, today announced that a significant development milestone has been reached with the completion of the facility and the transfer of MaaT Pharma’s Production and Development teams to the new site. The companies had entered a partnership in February 2022 to build the largest cGMP1 facility, to date, for full ecosystem microbiome therapies in Europe.
By MaaT Pharma · Via Business Wire · September 12, 2023
MaaT Pharma Announces European Medicines Agency Granted MaaT033 Orphan Drug Designation aiming to improve overall survival in patients undergoing Hematopoietic Stem Cell transplantation
Regulatory News:
By MaaT Pharma · Via Business Wire · September 7, 2023
MaaT Pharma Provides Second Quarter 2023 Business Update and Reports Financial Results
Regulatory News:
By MaaT Pharma · Via Business Wire · July 27, 2023
MaaT Pharma Announces Publication of Results in eClinicalMedicine Journal Highlighting Clinical Benefit of MaaT013 in aGvHD
Regulatory News:
By MaaT Pharma · Via Business Wire · July 26, 2023
MaaT Pharma Joins Microbiome Therapeutics Innovation Group
Regulatory News:
By MaaT Pharma · Via Business Wire · July 20, 2023
MaaT Pharma Announces New Appointments to the Board and Executive Team
Regulatory News:
By MaaT Pharma · Via Business Wire · June 21, 2023
MaaT Pharma Announces Cash and Revenues for the First Quarter of 2023
Regulatory News:
By MaaT Pharma · Via Business Wire · May 9, 2023
MaaT Pharma Announces U.S. FDA Lifts Clinical Hold on Phase 3 Investigational New Drug Application for MaaT013 in Patients with Acute Graft-versus-Host Disease
Regulatory News:
By MaaT Pharma · Via Business Wire · April 24, 2023
MaaT Pharma to Present Clinical Data for MaaT013 and MaaT033 at 49th EBMT Annual Meeting
Regulatory News:
By MaaT Pharma · Via Business Wire · April 11, 2023
MaaT Pharma Announces 2022 Annual Results and Provides a Business Overview
Regulatory News:
By MaaT Pharma · Via Business Wire · March 30, 2023
MaaT Pharma Receives Two Clinical Trial Application Authorizations to Evaluate MaaT033 in Two Therapeutic Indications in Europe
Regulatory News:
By MaaT Pharma · Via Business Wire · March 27, 2023
MaaT Pharma Announces Initiation of Coverage of its Stock by Kepler Cheuvreux
Regulatory News:
By MaaT Pharma · Via Business Wire · January 27, 2023
MaaT Pharma Provides Corporate Update and Highlights Key Expected Milestones in 2023
Regulatory News:
By MaaT Pharma · Via Business Wire · January 24, 2023
MaaT Pharma Presents Promising Detailed Results from Completed Phase 1b Trial with MaaT033 at the 64th ASH Annual Meeting
Regulatory News:
By MaaT Pharma · Via Business Wire · December 11, 2022
MaaT Pharma Presents Compelling Consolidated MaaT013 Clinical Data at the 64th ASH Annual Meeting
Regulatory News:
By MaaT Pharma · Via Business Wire · December 10, 2022
Articles from MaaT Pharma | MarketMinute