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consent\n\nExclusion Criteria:\n\n* Patients planned to receive a non-myeloablative conditioning regimen (2 Gray total body irradiation (TBI) +\u002F- purine analog, fludarabine + cyclophosphamide or equivalent)\n* Patients planned to receive a conventional myeloablative conditioning regimen (e.g. high dose cyclophosphamide and high dose TBI (≥10Gy); high dose busulfan (12.8 mg\u002Fkg IV) + high dose cyclophosphamide)\n* Patients receiving a manipulated graft (in-vitro T-cell depletion)\n* Patients planned to receive a conditioning regimen with alemtuzumab\n* Patients planned to receive alloHCT with cord blood cells\n* Patients planned to receive alloHCT from unrelated donor with \\>= 3\u002F10 HLA-mismatches\n* Patients receiving a large spectrum antibiotic at time of randomization\n* Patients planned to receive vedolizumab or abatacept for GvHD prophylaxis\n* Creatinine clearance \\\u003C30 mL\u002Fmin\n* Bilirubin or amino-transferases abnormalities contra-indicating alloHCT\n* Cardiac ejection fraction less than 40%\n* Pulmonary impairment with \\\u003C50% lung carbon monoxide diffusing capacity (DLCO)\n* Pregnancy\n* Confirmed or suspected intestinal ischemia\n* Confirmed or suspected toxic megacolon or gastrointestinal perforation\n* Any history of gastro-intestinal surgery in the past 3 months\n* Any history of chronic digestive disease (Crohn's disease, ulcerative colitis, inflammatory bowel disease or other relevant digestive condition according to physician's judgement)\n* Known allergy or intolerance to trehalose or maltodextrin\n* Patients with EBV-IgG negative serology\n* Any condition that would, in the investigator's judgment, interfere with full participation in the study, including administration of study drug and attending required study visits; pose a significant risk to the subject; or interfere with interpretation of study data.\n* Vulnerable patients such as: persons deprived of liberty, persons in Intensive Care Unit unable to provide informed consent prior to the intervention.","ALL","50 Years",{"count":652,"type":653},387,"ESTIMATED","INTERVENTIONAL",[656],"PHASE2","This randomized, placebo-controlled phase IIb study (PHOEBUS trial) aims to evaluate the activity of fecal microbiotherapy MaaT033 to improve survival through the prevention of transplant-related complications in eligible alloHCT patients",[659],"Transplant Complication","2024-12-20",{"date":662,"type":663},"2024-12-27","ACTUAL",{"date":665,"type":663},"2023-10-31",{"date":667,"type":653},"2027-02-15",{"name":5,"class":6},54]