Associated tags: Liver, Patient, Safety, Bone marrow, HSCT, Maat, Skin, Mortality, Biotechnology, ARES, Hematopoietic stem cell transplantation, Society, Sorbonne University, Execute Direct Access Program, Hospital, MET, Microbiota, Pharmaceutical, Cancer, Survival, Hematology, EAP, Graft-versus-host disease, Clinical Trials, Health, Pharmaceutical industry
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Pharmaceutical industry The data includes results from 24 patients in a Phase 2 clinical trial and 52 patients enrolled in the Early Access Program (EAP) in France.
Key Points:
- The data includes results from 24 patients in a Phase 2 clinical trial and 52 patients enrolled in the Early Access Program (EAP) in France.
- "Data show encouraging clinical outcomes and survival rates for very severe patients with acute GvHD, thereby opening new treatment avenues," said Pr.
- "Based on this promising clinical data, including the good tolerability and safety profile, we eagerly anticipate the results of the ongoing evaluation of MaaT013 in Phase 3."
- "The publication of our results in a peer-reviewed journal underlines the importance of the microbiome in the hematology-oncology field.
Retrieved on:
Saturday, December 7, 2019
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MaaT013,
MaaT Pharma MaaT Pharma announced today that leading hemato-oncological experts presented clinical data on the compassionate use of MaaT Pharmas lead full-ecosystem microbiome restoration biotherapeutic, MaaT013.
Key Points:
- MaaT Pharma announced today that leading hemato-oncological experts presented clinical data on the compassionate use of MaaT Pharmas lead full-ecosystem microbiome restoration biotherapeutic, MaaT013.
- The results were presented in a poster presentation on December7, 2019 during the 61st American Society of Hematology (ASH) Annual Meeting and Exposition held in Orlando, Florida.
- MaaT013 is the first full-ecosystem, off-the-shelf, reproducible, enema formulation manufactured using MaaT Pharmas integrated Microbiome Restoration Biotherapeutic (MMRB) platform.
- MaaT Pharma benefits from the commitment of world-leading scientists and established relationships with regulators to spearhead microbiome treatment integration into clinical practice.