to Evaluate MaaT033 in Two Therapeutic Indications in Europe.
MaaT Pharma (EURONEXT: MAAT – the “Company”), a French clinical-stage biotech and a pioneer in the development of Microbiome Ecosystem TherapiesTM (MET) dedicated to improving survival outcomes for patients with cancer, announced today that it has received regulatory authorizations for its two clinical trial applications evaluating MaaT033 in hemato-oncology and in amyotrophic lateral sclerosis (ALS).
French and German regulatory authorities for drugs and medical products, ANSM (Agence Nationale de Sécurité du Médicament et des Produits de Santé) and BfArM (Bundesinstitut für Arnzeimittel und Medizinprodukte) respectively, have authorized the application regarding the launch of the Company’s randomized, double-blind, placebo-controlled Phase 2b clinical trial evaluating MaaT033 in improving survival of patients with hematological malignancies receiving allo-HSCT. The Company also received authorization from ANSM, the French regulatory agency, to initiate its Phase 1b pilot study evaluating MaaT033 in slowing down disease progression in ALS. The Company will communicate on inclusion of the first patient in each study, which is expected by mid-2023.