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临床试验/NCT06201247
NCT06201247招募中早期 1 期

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

Peking University People's Hospital1 个研究点 分布在 1 个国家目标入组 12 人开始时间: 2023年12月30日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
早期 1 期
状态
招募中
入组人数
12
试验地点
1
主要终点
1-month DLTs

研究概览

简要总结

This is a single-centre, single-arm, open-label, first-in-human (FIH) study to evaluate the safety, tolerability and preliminary 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 (AML).

详细描述

This is a dose-escalation study of CD123-targeted chimeric antigen receptor modified natural killer cells (CAR-NK) derived from a healthy donor. The relapsed/refractory AML patients will receive FC (F, Fludarabine, C, Cyclophosphamide) chemotherapy followed by infusion of JD123 injections. No graft-versus-host disease (GVHD) prevention will be conducted before or after infusion. Dose-limiting toxicity, incidence of adverse events, disease response and PK/PD will be detected post-infusion.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • 未提供

排除标准

  • 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;
  • Known alcohol dependence or drug dependence;
  • According to the investigator's judgment, the patient has other unsuitable grouping conditions.

研究组 & 干预措施

Experimental: Experimental: JD123 injection.

Experimental

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.

干预措施: JD123 injection (Drug)

结局指标

主要结局

1-month DLTs

时间窗: 1-month

Dose limiting toxicities (DLTs)

次要结局

  • 1-year PFS(1-year)
  • 3-month Peak(3-month)
  • 3-month CR/CRi(3-month)
  • 1-year OS(1-year)
  • 1-year MRD(-)(1-year)
  • 3-month AUC(3-month)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Xiao-Jun Huang

Professor

Peking University People's Hospital

研究点 (1)

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