Study of KITE-222 in Participants With Relapsed/Refractory Acute Myeloid Leukemia

Exclusion Criteria

• •Diagnosis of acute promyelocytic leukemia
• •Auto-SCT within the 6 weeks before enrollment
• •Donor Lymphocyte Infusions (DLI) within 28 days prior to enrollment
• •Any drug used for graft-versus-host-disease (GVHD) within 4 weeks prior to enrollment
• •Acute GVHD grade II-IV by Mount Sinai Acute GVHD International Consortium criteria
• •Active central nervous system (CNS) disease involvement
• •Requirement for urgent therapy due to ongoing or impending oncologic emergency (eg, leukostasis or tumor lysis syndrome (TLS)) or the possible requirement for urgent therapy due to ongoing or impending oncologic emergency (eg, spinal cord compression, bowel obstruction, leukostasis, or TLS) at the time of enrollment or KITE-222 infusion
• •History of C-type lectin-like molecule-1 (CLL-1)-directed therapy or genetically modified T-cell therapy
• •History of malignancy other than nonmelanoma skin cancer or carcinoma in situ (eg, cervix, bladder, or breast) unless disease free for at least 3 years after the last definitive therapy
• •History of severe hypersensitivity reaction to aminoglycosides
• •History of concomitant genetic syndrome associated with bone marrow failure
• •Individuals with a genetic syndrome that increases the risk of allo-SCT, including Down syndrome (trisomy 21)
• •History of myocardial infarction, cardiac angioplasty or stenting, unstable angina, New York Heart Association Class II or greater congestive heart failure, atrial fibrillation, or other clinically significant cardiac disease within 12 months before enrollment
• •Individuals with cardiac atrial or ventricular leukemia involvement
• •History of symptomatic deep vein thrombosis (DVT) or a pulmonary embolism within 6 months of enrollment. History of upper extremity line related DVT within the 3 months of conditioning chemotherapy.
• •Primary immunodeficiency disorders
• •History of a human immunodeficiency virus (HIV) infection or acute or chronic active hepatitis B or C infection
• •History of an autoimmune disease resulting in end-organ injury or requiring systemic immunosuppression or systemic disease modifying agents within the last 2 years
• •History or presence of a CNS disorder
• •Presence or suspicion of a fungal, bacterial, viral, or other infection that is uncontrolled or requiring antimicrobials for management
• •Live vaccine received within the ≤ 4 weeks before enrollment, or anticipation of the need for a live vaccination during the course of the study
• •Inability to tolerate prophylactic antifungal and antibacterial therapy
• •Presence of any indwelling line or drain
• •Ongoing Grade 2 or higher toxicities from previous therapies, excluding hematologic toxicities
• •Females of childbearing potential who are pregnant or breastfeeding