Trial Radar AI | ||
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Clinical Trial NCT06201247 for Acute Myeloid Leukemia, in Relapse, Acute Myeloid Leukemia Refractory is recruiting. See the Trial Radar Card View and AI discovery tools for all the details. Or ask anything here. | ||
Off-the-shelf CD123 CAR-NK for R/R AML Early Phase 1 12 First-in-Human Open-Label
Safety and Efficacy of Universal Off-the-shelf CAR-NK Cells Targeted CD123 (JD123 Injection) in the Treatment of Refractory or Relapsed CD123-positive Acute Myeloid Leukemia
- 2023PHD016-001
CAR-NK
| Participant Group/Arm | Intervention/Treatment |
|---|---|
ExperimentalExperimental: Experimental: JD123 injection. The relapsed/refractory AML patients will receive JD123 injections up to 3 dose levels (5.0×108 cells/dose，1.5×109 cells/dose，3.0×109 cells/dose) after FC chemotherapy. | JD123 injection JD123 injection is an universal Off-the-shelf CD123-targeted chimeric antigen receptor modified natural killer cells (CAR-NK) therapy derived from a healthy donor. |
| Outcome Measure | Measure Description | Time Frame |
|---|---|---|
1-month DLTs | Dose limiting toxicities (DLTs) | 1-month |
| Outcome Measure | Measure Description | Time Frame |
|---|---|---|
3-month CR/CRi | Complete response (CR) or Complete remission with incomplete recovery(CRi) | 3-month |
1-year PFS | Progression free survival(PFS) | 1-year |
1-year OS | Overall Survival (OS) | 1-year |
1-year MRD(-) | Proportion of subjects with minimal-residual disease (MRD) negative response | 1-year |
3-month AUC | The area under the concentration time-curve (AUC) of CD123-CAR-NK cells | 3-month |
3-month Peak | Peak levels of CD123-CAR-NK cells (maximum concentration or Cmax) | 3-month |
Age ≥ 18 years old, no gender or race;
Expected survival period ≥ 3 months;
Eastern Cooperative Oncology Group (ECOG) performance status score of 0 to 2;
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.
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.
- Active Central nervous system leukemia;
- Known contraindication to the protocol defined lymphodepleting chemotherapy regimen of fludarabine/cyclophosphamide;
- Systemic use of hormones within 4 weeks prior to enrollment (except for patients with inhaled corticosteroids);
- 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.
- History of hypersensitivity reactions to murine protein-containing products, or macromolecular biopharmaceuticals such as antibodies or cytokines;
- Patients cannot guarantee effective contraception (condom or contraceptives, etc.) within 1 years after enrollment;
- Women who are pregnant (urine/blood pregnancy test positive) or lactating;
- 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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Peking University People's HospitalBeijing Municipality