Clinical Research Directory

Inclusion Criteria: 1. Patients with AML who completed Hikma bioequivalence study of the same Hikma generic oral Azacitidine test product with protocol number: HIK-AZA-2023-01, and who consent to participate in the study. 2. Patients who understand and voluntarily sign a written informed consent document prior to any study related assessment/procedures are conducted. Exclusion Criteria: 1. Female patients who are pregnant or nursing (lactating). 2. Patients with medical condition, laboratory abnormality, or psychiatric illness that, in the opinion of the investigator, might interfere with subject safety, compliance or evaluation of the condition of the study. 3. Patients with experience in any investigational drug in a clinical study within 6 months prior to study (except for patients who were enrolled in the Hikma Azacitidine bioequivalence study with protocol number: HIK-AZA-2023-01).