This phase I trial studies the side effects and best dose of CART123 when given alone or together with ruxolitinib and to see how well it works in treating patients with acute myeloid leukemia (AML) that has come back after a period of improvement (relapsed) or that does not respond to treatment (refractory). CART123 is a type of chimeric antigen receptor (CAR) T-cell therapy. CAR T-cell therapy is a treatment in which a patient's T cells (a type of immune system cell) are changed in the laboratory so they will attack cancer cells. T cells are taken from a patient's blood. Then the gene for a special receptor that binds to a certain protein on the patient's cancer cells is added to the T cells in the laboratory. The special receptor is called a CAR. Large number of the CAR T cells are grown in the laboratory and given to the patient by infusion. Ruxolitinib may stop the growth of cancer cells by blocking some of the enzymes needed for cell growth. Giving CART123 alone or together with ruxolitinib may be safe, tolerable, and/or effective in treating patients with relapsed or refractory AML.
Study sponsor and potential other locations can be found on ClinicalTrials.gov for NCT07464951.
Locations matching your search criteria
United States
Pennsylvania
Philadelphia
Children's Hospital of PhiladelphiaStatus: Active
Contact: Lucy Ellen Cain
Phone: 215-590-2299
PRIMARY OBJECTIVES:
I. Evaluate the safety of autologous anti-CD123 CAR-T cells (CART123). (Cohort A)
II. Evaluate the safety of CART123 cells given in combination with ruxolitinib. (Cohort B)
SECONDARY OBJECTIVES:
I. To determine the feasibility of CART123 treatment. (Cohort A)
II. To determine the feasibility of combining CART123 and ruxolitinib. (Cohort B)
III. To describe preliminary efficacy assessed separately for each cohort.
IV. To evaluate the need for rescue allogeneic hematopoietic stem cell transplant assessed separately for each cohort.
EXPLORATORY OBJECTIVES:
I. To describe the expansion and persistence of CART123 cells. (Cohort A)
II. To describe the expansion and persistence of CART123 cells given in combination with ruxolitinib. (Cohort B)
III. To evaluate the bioreactivity of CART123 cells. (Cohort A)
IV. To evaluate the bioreactivity of combination therapy. (Cohort B)
OUTLINE: This is a dose-escalation study of CART123 cells (Cohort A) followed by a fixed dose study of CART123 cells in combination with ruxolitinib (Cohort B). Patients are assigned to 1 of 2 cohorts.
COHORT A: Patients undergo apheresis for the manufacturing of CART123 cells during week -4 to -3. Patients then receive lymphodepleting chemotherapy consisting of fludarabine for 4 days and cyclophosphamide for 2 days from days -5 to -2. After the completion of lymphodepleting chemotherapy, patients receive CART123 cells intravenously (IV) on day 0 in the absence of disease progression or unacceptable toxicity. Patients who achieve at least a partial response after initial CART123 infusion may be retreated with CART123 cells with or without lymphodepleting chemotherapy for up to 3 additional infusions or crossover to Cohort B at the investigator's discretion.
COHORT B: Patients undergo apheresis for the manufacturing of CART123 cells during week -4 to -3. Patients then receive lymphodepleting chemotherapy consisting of fludarabine for 4 days and cyclophosphamide for 2 days from days -5 to -2. After the completion of lymphodepleting chemotherapy, patients receive CART123 cells IV on day 0. Additionally, patients receive ruxolitinib orally (PO) once daily (QD) or twice daily (BID) from the start of lymphodepleting chemotherapy until day -2 and again on day +7 to day +13 in the absence of disease progression or unacceptable toxicity. Ruxolitinib may continue or be given later in the post-CART123 course at the investigator's discretion. Patients who achieve at least a partial response after initial CART123 infusion may be retreated with CART123 cells in combination with ruxolitinib with or without lymphodepleting chemotherapy for up to 3 additional infusions or crossover to Cohort A at the investigator's discretion.
Additionally, all patients undergo echocardiography (ECHO) during screening and positron emission tomography (PET)/computed tomography (CT) or PET/magnetic resonance imaging (MRI) as clinically indicated throughout the study. Patients may also undergo blood and/or cerebrospinal fluid (CSF) sample collection as well as bone marrow aspiration and biopsy throughout the study.
After completion of study treatment, patients are followed up either at days 1, 3, 7, 10, 14, 21, and 28 (Cohort A) or days 14, 21, and 28 (Cohort B), and then monthly during months 2-6. Patients may then be optionally followed for up to 15 years on separate long term follow-up protocol.
Lead OrganizationChildren's Hospital of Philadelphia
Principal InvestigatorLucy Ellen Cain