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Allogeneic CAR-T(CT0890B) in NKG2DL+ R/R AML

2026年5月23日 更新者:Xiangyu Zhao、Peking University People's Hospital

A Phase I Study to Evaluate the Safety and Efficacy of Allogeneic CAR-T Cells (CT0890B) in Patients With NKG2DL-Positive Relapsed/Refractory Acute Myeloid Leukemia

A Clinical Study to Investigate the Safety and Efficacy of CT0890B in Patients with Relapsed/Refractory Acute Myeloid Leukemia.

研究概览

详细说明

This is a single-arm, open-label, dose-escalation clinical trial to evaluate the safety, efficacy, and cellular pharmacokinetics of CT0890B in patients with relapsed or refractory acute myeloid leukemia. It is planned to enroll 12~27 participants in this trial.

研究类型

介入性

注册 (估计的)

27

阶段

  • 阶段1

联系人和位置

本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。

学习联系方式

研究联系人备份

学习地点

      • Beijing、中国、100044
        • 招聘中
        • Peking University People's Hospital
        • 副研究员:
          • Meng Lv, M.D, Ph.D
        • 接触:
        • 首席研究员:
          • Xiangyu Zhao, M.D, Ph.D

参与标准

研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。

资格标准

适合学习的年龄

  • 成人
  • 年长者

接受健康志愿者

不

描述

Inclusion Criteria:

  1. Age 18-70 years (inclusive), male or female.
  2. Relapsed or refractory acute myeloid leukemia (R/R AML) diagnosed according to the 2022 World Health Organization classification or ELN criteria, with confirmed NKG2D ligand-positive disease.
  3. Bone marrow blasts ≥5% by morphology.
  4. Estimated life expectancy >12 weeks.
  5. Eastern Cooperative Oncology Group (ECOG) performance status of 0-2.
  6. Adequate organ function without ongoing supportive care, defined as:

    1. Cardiac: left ventricular ejection fraction (LVEF) ≥50%;
    2. Hepatic: ALT and AST ≤2.5 × upper limit of normal (ULN), and total bilirubin ≤2 × ULN;
    3. Renal: creatinine clearance ≥30 mL/min (calculated using the Cockcroft-Gault formula);
    4. Coagulation: activated partial thromboplastin time (APTT) ≤1.5 × ULN and prothrombin time (PT) ≤1.5 × ULN.

    c) Renal: creatinine clearance ≥30 mL/min (calculated using the Cockcroft-Gault formula); d) Coagulation: activated partial thromboplastin time (APTT) ≤1.5 × ULN and prothrombin time (PT) ≤1.5 × ULN.

Exclusion Criteria:

  1. Participants were diagnosed with acute promyelocytic leukemia (APL), BCR-ABL positive leukemia (chronic myeloid leukemia in acute phase), central nervous system leukemia;
  2. Participants with a history of epilepsy or other central nervous system disease;
  3. Participants who have previously received autologous or allogeneic CAR-T therapy;
  4. Participants who have received autologous stem cell transplantation or allogeneic stem cell transplantation within 12 weeks
  5. Participants who have received prior immunotherapy targeting NKG2DL;
  6. Participant has clinically significant active GVHD or is receiving systemic corticosteroids for GVHD;
  7. Participant has any of the following at screening:

1)Active, uncontrolled systemic infection or requiring intravenous anti-infective agents 2)Any of the following cardiac conditions, including:

  1. New York Heart Association Class III-IV heart failure;
  2. History of myocardial infarction, coronary artery bypass grafting, or unstable angina within 6 months prior to Qinglin;
  3. History of uncontrolled arrhythmia of significant clinical significance (as judged by the investigator), such as ventricular arrhythmia;
  4. History of severe nonischemic ardiomyopathy;
  5. Other cardiac disease that the investigatorbelieve could jeopardize the participant 's well-being or compromise participation in this clinical trial; 3) Active bleeding of clinical significance as judged by the investigator; 4)Requiring supplemental oxygen to maintain oxygen saturation> 92%; 5)Patients with severe chronic obstructive pulmonary disease (COPD) or other lung diseases that cannot tolerate CAR-T treatment as judged by the investigator;

学习计划

本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。

研究是如何设计的?

设计细节

  • 主要用途:治疗
  • 分配:不适用
  • 介入模型:单组作业
  • 屏蔽:无(打开标签)

武器和干预

参与者组/臂
干预/治疗
实验性的:CAR-T cells chimeric antigen receptor T cells
CT0890B cells infusion

Conditioning regimen:

Days -9 to -3:

Venetoclax administered with a target dose of 200 mg/day.

Days -5 to -4:

Cytarabine administered at 500 mg/m²/day.

Days -5 to -3:

Cyclophosphamide at 300 mg/m²/day plus Fludarabine at 30 mg/m²/day.

Day 0:

Infusion of CT0890B CAR-T cells at one of four dose levels using an i3+3 Dose-Escalation Design:

1.5 × 10⁸ total cells, 3.0 × 10⁸ total cells, 4.5 × 10⁸ total cells, 6.0 × 10⁸ total cells

其他名称:
  • Off-the-shelf allogeneic CAR-T cells

研究衡量的是什么?

主要结果指标

结果测量
措施说明
大体时间
Adverse Events (AE) after CT0890B infusion
大体时间:12 months after CT890B infusion
An assessment of severity grade will be made according to the National Cancer Institute Common Terminology Criteria
12 months after CT890B infusion
Dose-limiting toxicity (DLT)
大体时间:Up to 28 days after CAR-T cells infusion
The DLT is evaluated as the proportion of patients who experienced adverse events related to CT0890B that meet the criteria for DLT events after the first infusion
Up to 28 days after CAR-T cells infusion
MTD and/or dose range
大体时间:Up to 28 days after CAR-T cells infusion
Evaluate Dose limited toxicity and recommended dosage range after CT0890B infusion
Up to 28 days after CAR-T cells infusion

次要结果测量

结果测量
措施说明
大体时间
Composite response (CRc)
大体时间:12 months after CT0890B infusion
The composite response rate (CRc) included complete response (CR), complete response with partial hematologic recovery (CRh), complete response with incomplete hematologic recovery (CRi), and morphologic leukemia-free state (MLFS). Responses were assessed in accordance with the Technical Guidelines for Clinical Development of New Drugs for Acute Myeloid Leukemia and the 2022 European LeukemiaNet criteria for acute myeloid leukemia (AML).
12 months after CT0890B infusion
Partial response (PR)
大体时间:12 months after CT0890B infusion
Partial response (PR) was defined and assessed according to the Technical Guidelines for Clinical Development of New Drugs for Acute Myeloid Leukemia and the 2022 European LeukemiaNet response criteria for AML.
12 months after CT0890B infusion
Rate of Subsequent Stem Cell Transplantation After CAR-T Therapy
大体时间:12 months after CT0890B infusion
This secondary endpoint was defined as the proportion of patients who proceeded to stem cell transplantation after CAR-T therapy during the study period.
12 months after CT0890B infusion
Duration of response (DOR)
大体时间:12 months after CT0890B infusion
Patients achieving CR, CRi, CRh, or MLFS were included in the duration of response (DOR) analysis set. DOR was defined as the time from the date of first documented response to the date of disease relapse or death from any cause, whichever occurred first.
12 months after CT0890B infusion
Event-free survival (EFS)
大体时间:12 months after CT0890B infusion

EFS was defined as the time from the date of CAR-T infusion to the earliest occurrence of treatment failure, relapse, or death from any cause. Treatment failure was defined as failure to achieve CR, CRh, CRi, MLFS, or PR at both prespecified efficacy assessments. Relapse included hematologic or extramedullary relapse after achieving CR, CRh, CRi or MLFS.

For patients with treatment failure (ineffective therapy), the primary EFS analysis assigned an event time of 1 day (i.e., the time from infusion to treatment receipt). Sensitivity analyses were performed using alternative definitions of event timing, including the actual date of treatment failure, the end of treatment, or the initiation of subsequent anti-leukemia therapy.

12 months after CT0890B infusion
Overall survival (OS)
大体时间:12 months after CT0890B infusion
OS is defined as the time from the date of receiving the infusion to the date of death from any cause.
12 months after CT0890B infusion
Minimal Residual Disease (MRD) Negativity Rate
大体时间:12 months after CT0890B infusion
MRD negativity rate was assessed in participants who achieved CR, CRh, CRi or MLFS. MRD negativity was defined as <0.01% abnormal cells among CD45-positive cells as determined by multiparameter flow cytometry (MFC).
12 months after CT0890B infusion
Pharmacokinetic Endpoint - Peak expansion (Cmax)
大体时间:12 months after CT0890B infusion
The maximum concentration or peak value of CT0890B cells in plasma after infusion, measured by CAR copy number.
12 months after CT0890B infusion
Time to peak expansion (Tmax) of CT0890B
大体时间:12 months after CT0890B infusion
The time required to reach the peak expansion (maximum CAR copy number) in plasma following the infusion of CT0890B cells.
12 months after CT0890B infusion
Area under the curve (AUC) of CT0890B
大体时间:12 months after CT0890B infusion
The total cellular exposure in plasma after infusion, calculated based on the area under the CAR copy number-time curve.
12 months after CT0890B infusion
In vivo persistence of CT0890B
大体时间:Up to 12 months after CT0890B infusion
The duration for which CT0890B cells remain detectable in the plasma after infusion, monitored via CAR copy number.
Up to 12 months after CT0890B infusion

合作者和调查者

在这里您可以找到参与这项研究的人员和组织。

调查人员

  • 首席研究员:XiangYu Zhao, M.D, Ph.D、Peking University People's Hospital

研究记录日期

这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。

研究主要日期

学习开始 (估计的)

2026年5月7日

初级完成 (估计的)

2027年12月31日

研究完成 (估计的)

2029年12月31日

研究注册日期

首次提交

2026年5月1日

首先提交符合 QC 标准的

2026年5月23日

首次发布 (实际的)

2026年6月1日

研究记录更新

最后更新发布 (实际的)

2026年6月1日

上次提交的符合 QC 标准的更新

2026年5月23日

最后验证

2026年5月1日

更多信息

与本研究相关的术语

其他研究编号

  • CT0890B-CG8001

计划个人参与者数据 (IPD)

计划共享个人参与者数据 (IPD)?

未定

药物和器械信息、研究文件

研究美国 FDA 监管的药品

不

研究美国 FDA 监管的设备产品

不

此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.

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