APVO436 Phase 1b/2 Study in Patients With Newly Diagnosed AML

Eligibility Criteria

• * 1. Age ≥18 years. 2. Patient must have confirmation of AML based on 2016 World Health Organization (WHO) criteria and not been previously treated.
• 3. Patients must have CD123-positive AML as confirmed by local flow cytometry (or immunohistochemistry \[IHC\]). Confirmation at diagnosis is acceptable.
• 4. Patient must be considered ineligible for induction therapy defined by at least one of the following:
• 1. ≥75 years of age
• 2. Eastern Cooperative Oncology Group (ECOG) Performance Status of 2 or 3
• 3. Cardiac disorder (e.g., congestive heart failure requiring treatment, ejection fraction ≤ 50%, or chronic stable angina)
• 4. Pulmonary disorder (e.g., DLCO ≤65% or FEV1 ≤65%)
• 5. Creatinine clearance 30-45 mL/min based on Cockcroft-Gault or Modified of Diet in Renal Disease (MDRD) formular
• 6. Hepatic disorder with total bilirubin between 1.5 and 3 times the ULN 5. Patient must have a projected life expectancy of ≥12 weeks
• 1. Patient has received treatment with the following:
• 1. A hypomethylating agent, venetoclax, and/or chemotherapeutic agent for AML, myelodysplastic syndrome (MDS), chronic myelomonocytic leukemia (CMML), or myelodysplastic/myeloproliferative neoplasms (MPS/MPN)
• 2. CAR-T cell therapy or history of allogeneic hematopoietic stem cell transplant (HSCT)
• 3. Experimental therapies for MDS or AML
• 2. Patient is currently participating in another interventional research study.
• 3. Patient has history of MPN including myelofibrosis, essential thrombocythemia, polycythemia vera, chronic myeloid leukemia (CML) with or without BCR-ABL1 translocation, or AML with BCR-ABL1 translocation.
• 4. Patient has acute promyelocytic leukemia.
• 5. Patient has a current autoimmune disorder requiring immunosuppressive therapy such as systemic (oral or IV) steroid therapy \>10 mg methylprednisolone daily or its equivalent
• 6. Patient is receiving concurrent corticosteroid therapy as an anticancer drug (any dose).
• 7. Patient has known active CNS involvement with AML. Patients who received intrathecal chemotherapy for prophylaxis of AML in the CNS prior to enrollment may enroll in this study.
• 8. Creatinine clearance \<30ml/min based on Cockcroft-Gault or MDRD formular.
• 9. Bilirubin of \>3xULN in the absence of Gilbert's Syndrome.
• 10. AST and/or ALT \>3 times the ULN.