Off-the-shelf CD123 CAR-NK for R/R AML

Launched by PEKING UNIVERSITY PEOPLE'S HOSPITAL · Dec 30, 2023

Keywords

ClinConnect Summary

This clinical trial is studying a new treatment called JD123 injection, which uses specially engineered immune cells (CAR-NK cells) to target and fight acute myeloid leukemia (AML) that has either come back after treatment (relapsed) or hasn’t responded to standard therapies (refractory). The goal is to see how safe and effective this new treatment is for patients with AML that has a specific marker called CD123.

To be eligible for this trial, participants must be at least 18 years old and have a confirmed diagnosis of CD123-positive AML. They should also be expected to live at least three more months and have certain health criteria, like functioning organs. Participants will receive the new treatment and will be monitored closely for any side effects and how well the treatment works. It's important to note that women who can become pregnant and all men need to use effective contraception during the study and for a year afterward. This study is currently recruiting participants, and it offers an opportunity to help advance new options for those facing challenging cases of leukemia.

Gender

ALL

Eligibility criteria

• Inclusion criteria:
• • 1. Age ≥ 18 years old, no gender or race;
• • 2. Expected survival period ≥ 3 months;
• • 3. Eastern Cooperative Oncology Group (ECOG) performance status score of 0 to 2;
• 4. The diagnosis of AML with bone marrow biopsy, immunohistochemistry or Flow cytometry definitively positive for CD123 and met the following criteria:
• • A. Diagnostic criteria for relapsed AML: after complete remission (CR), leukemia cells reappeared in peripheral blood or blast cells in bone marrow ≥ 5% (except for other reasons such as bone marrow regeneration after consolidation chemotherapy) or extramedullary leukemia cell infiltration; B. Diagnostic criteria for refractory AML: naive patients who were ineffective after 2 courses of standard regimens; patients relapsed within 12 months who underwent consolidation and intensive therapy after CR; patients relapsed after 12 months but were ineffective after conventional chemotherapy; Patients with two or more relapses; patients with persistent extramedullary leukemia; Patients relapsed after allogeneic hematopoietic stem cell transplantation (allo-HSCT) C. Minimal Residual Disease (MRD) positive only or relapse: Patient is minimal residual disease (MRD) positive, as assessed on bone marrow aspirate (BMA) by Multiparameter Flow Cytometry (MFC) at time of Treatment Eligibility assessment.
• 5. Adequate organ function:
• • A. Liver function: ALT≤3×ULN, AST≤3×ULN, total bilirubin≤2×ULN; B. Coagulation function: international normalized ratio (INR) or activated partial thromboplastin time (APTT) ≤ 1.5×ULN; C. Renal function: serum creatinine≤1.5×ULN or creatinine clearance rate ≥30mL/min; D. Cardiac function: Left ventricular ejection fraction (LVEF) ≥ 50%; 6. Women of child-bearing potential and all male participants must use effective methods of contraception for at least 12 months after infusion.; 7. Informed Consent/Assent: All subjects must have the ability to understand and the willingness to sign a written informed consent.
• Exclusion Criteria:
• • 1. Active Central nervous system leukemia;
• • 2. Known contraindication to the protocol defined lymphodepleting chemotherapy regimen of fludarabine/cyclophosphamide;
• • 3. Systemic use of hormones within 4 weeks prior to enrollment (except for patients with inhaled corticosteroids);
• • 4. Any active infection requiring systemic therapy by intravenous infusion within 14 days prior to the first dose of study drug, including: HBV, HCV, HIV, syphilis infection, or active pulmonary tuberculosis.
• • 5. History of hypersensitivity reactions to murine protein-containing products, or macromolecular biopharmaceuticals such as antibodies or cytokines;
• • 6. Patients cannot guarantee effective contraception (condom or contraceptives, etc.) within 1 years after enrollment;
• • 7. Women who are pregnant (urine/blood pregnancy test positive) or lactating;
• • 8. Suffering from a serious autoimmune disease or immunodeficiency disease; 9 Suffering from mental illness;
• • 10. Known alcohol dependence or drug dependence; 11. According to the investigator's judgment, the patient has other unsuitable grouping conditions.
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