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Participation in another post-marketing observational study or Registry is acceptable","ALL","18 Years",{"count":291,"type":292},150,"ESTIMATED","OBSERVATIONAL","Acute myeloid leukemia (AML) is a cancer of the blood and bone marrow and is the most common acute leukemia in adults. This study will evaluate how well venetoclax in combination with azacitidine works to treat AML in newly diagnosed adult participants who are ineligible for intensive chemotherapy in Italy.\n\nVenetoclax in combination with azacitidine is approved in Italy to treat Acute myeloid leukemia (AML) in newly diagnosed adults who are ineligible for intensive chemotherapy. All study participants will receive venetoclax in combination with azacitidine as prescribed by their study doctor in accordance with approved local label. Adult participants with a new diagnosis of AML will be enrolled. Around 150 participants will be enrolled in the study at approximately 20-25 sites in Italy.\n\nParticipants will receive venetoclax tablets to be taken by mouth in combination with azacitidine given by subcutaneous (SC) injection according to the approved local label. The duration of the study is approximately 18 months.\n\nThere is expected to be no additional burden for participants in this trial. All study visits will occur during routine clinical practice and participants will be followed for 18 months.",[296],"Acute Myeloid Leukemia",[296,298,299,300,301,302,303],"Venetoclax","Venclexta","Venclyxto","Azacitidine","ABT-199","Cancer","ACTIVE_NOT_RECRUITING","2025-04-18",{"date":307,"type":308},"2025-04-22","ACTUAL",{"date":310,"type":308},"2024-03-04",{"date":312,"type":292},"2026-11",{"name":5,"class":6},28]