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META 10-19 in Patients With Relapsed/Refractory Autoimmune Hemolytic Anemia

2026年7月6日 更新者:Jun Shi、Institute of Hematology & Blood Diseases Hospital, China

Phase I Clinical Study on the Safety and Tolerability of META 10-19 Infusion in Patients With Relapsed/Refractory Autoimmune Hemolytic Anemia

A Study of Metabolically Armed Autologous CD19 CAR T-Cell Therapy (META 10-19) in Patients with Relapsed/Refractory Autoimmune Hemolytic Anemia

研究概览

详细说明

This is a Phase I clinical study evaluating metabolically armed autologous CD19 CAR T-cell therapy (META 10-19) in patients with relapsed/refractory autoimmune hemolytic anemia (AIHA). The main purpose of this study is to assess the safety and tolerability of this therapy in patients with relapsed/refractory AIHA.

-Primary Objective: To evaluate the safety and tolerability of metabolically armed autologous CD19 CAR T-cell therapy (META 10-19) in patients with relapsed/refractory autoimmune hemolytic anemia (AIHA).

-Secondary Objectives:

  1. To evaluate the preliminary efficacy of metabolically armed autologous CD19 CAR T-cell therapy (META 10-19) in study participants with relapsed/refractory AIHA.
  2. To assess the pharmacokinetic (PK) and pharmacodynamic (PD) characteristics of the metabolically armed autologous CD19 CAR T-cell therapy (META 10-19).

研究类型

介入性

注册 (估计的)

18

阶段

  • 第一阶段早期

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

学习地点

    • Tianjin Municipality
      • Tianjin、Tianjin Municipality、中国、300000
        • Blood Diseases Hospital, Chinese Academy of Medical Sciences
        • 首席研究员:
          • Jun Shi
        • 接触:
        • 副研究员:
          • Ruonan Li

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:

  • Aged 18 to 75 years, regardless of genders.
  • Diagnosis of AIHA (including warm antibody type, mixed warm and cold antibody type, cold agglutinin disease) or Evans syndrome, consistent with the Chinese Expert Consensus on the Diagnosis and Treatment of Autoimmune Hemolytic Anemia (2023), or the Diagnosis and Treatment of Autoimmune Hemolytic Anemia in Adults: Recommendations from the First International Consensus Meeting (Blood Rev, 2020), or the Chinese Expert Consensus on the Diagnosis and Treatment of Evans Syndrome (2024 Edition).
  • Definition of relapsed/refractory disease, meeting all of the following criteria:

    1. Hemoglobin < 10 g/dL with clinical manifestations of hemolytic anemia;
    2. After treatment with at least two immunosuppressive agents (which must include an anti-CD20 monoclonal antibody, with a cumulative dose of the anti-CD20 antibody reaching at least 375 mg/m² × 4, or a total dose of 2.0 g, or at least 6 cumulative administrations with an interval of ≥1 week between each);
    3. Glucocorticoid therapy for no less than 3 months (except for those with comorbidities that contraindicate corticosteroid use, severe infection, severe osteoporosis, previous fractures, or intolerance to glucocorticoids).
  • Eastern Cooperative Oncology Group (ECOG) performance status score ≤ 2;
  • Estimated life expectancy ≥12 weeks;
  • Adequate organ function as assessed by laboratory tests: Serum alanine aminotransferase (ALT) and aspartate aminotransferase (AST) ≤ 3 × upper limit of normal (ULN); and minimal pulmonary reserve, defined as dyspnea ≤ grade 1 and oxygen saturation ≥ 93% while breathing room air; creatinine clearance (estimated by Cockcroft-Gault) ≥ 45 mL/min; cardiac ejection fraction ≥ 50%, with no signs of pericardial effusion on echocardiography (ECHO) and no clinically significant electrocardiogram (ECG) abnormalities.
  • During the study period (from the signing of this informed consent form until at least 12 months after META 10-19 infusion, and until two consecutive PCR tests show no detectable CAR-T cells in the body), the study participant and their spouse/partner must use appropriate and effective contraceptive measures (excluding rhythm method/calendar-based contraception).
  • Study participants must sign a written informed consent form approved by the Ethics Committee prior to the initiation of any screening procedures.

Exclusion Criteria:

  • Previously diagnosed definite lymphoproliferative neoplasms; other malignant tumors within the past 5 years (excluding cured basal cell carcinoma of the skin, squamous cell carcinoma of the skin, superficial bladder cancer, breast carcinoma in situ, and cervical carcinoma in situ).
  • Secondary AIHA caused by drugs or infection.
  • Presence of active hepatitis or a history of severe liver disease or condition during the screening period:

    1. Hepatitis B: HBsAg or HBeAg positive; or hepatitis B e antibody (HBe-Ab) and/or hepatitis B core antibody (HBc-Ab) positive with HBV-DNA copy number above the lower limit of detection.
    2. Hepatitis C: Anti-HCV positive and HCV RNA ≥ lower limit of quantification (LLoQ).
    3. Human immunodeficiency virus (HIV) antibody positive.
    4. Active syphilis infection (excluding those with only positive syphilis-specific antibodies).
  • Previous history of organ transplantation or hematopoietic stem cell transplantation.
  • Severe cardiovascular diseases:

    1. Cardiovascular disease with New York Heart Association (NYHA) class > 2 within 6 months prior to the first study drug administration.
    2. Unstable angina or severe arrhythmia requiring medication, including QTcF > 480 ms (calculated by Fridericia's formula).
    3. Other significant electrocardiogram (ECG) abnormalities, including second-degree type II atrioventricular block, third-degree atrioventricular block, bradycardia (ventricular rate < 50 bpm with clinical symptoms), etc.
    4. Myocardial infarction within the past 6 months.
    5. Other cardiac diseases considered unsuitable for enrollment by the investigator.
  • Undergone major surgery within the past 4 weeks that is deemed by the investigator as unsuitable for enrollment.
  • Presence of active infection (e.g., sepsis, bacteremia, fungemia, uncontrolled pulmonary infection, active tuberculosis, etc.); active infection requiring intravenous anti-infective therapy within 7 days prior to screening.
  • Receipt of CAR T-cell therapy within 6 months prior to screening, or positivity for ADA, or positivity for HAMA, or receipt of in vivo CAR T-cell therapy within the previous 6 months; or a history of severe immediate hypersensitivity reaction to any cellular product, excipients, or related drugs used in this study.
  • Individuals with a history of epilepsy or other active central nervous system diseases (including but not limited to cerebrovascular accident, cerebral hemorrhage, cerebral infarction, severe traumatic brain injury, dementia, organic brain syndrome, etc.).
  • Women with a positive pregnancy test or who are breastfeeding; women of childbearing potential and all male study participants who are unwilling or unable to use effective contraceptive methods during the study period and for at least 12 months after study drug infusion.
  • Any other condition or circumstance that, in the investigator's opinion, would make the participant unsuitable for participation in this study.

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:META 10-19 CAR T-Cell Therapy
Participants will receive META 10-19 CAR T-cell infusion. Participants will be closely monitored for 24 hours after infusion. Hospitalization for a minimum of 14 days after infusion is recommended. The duration of hospitalization and observation will be determined based on the investigator's clinical assessment of the participant's condition.
Metabolically Armed Autologous CD19 CAR T-cells. Each subject receive metabolically autologous armed CD19 CAR T-cells by intravenous infusion.
其他名称:
  • META 10-19

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
Incidence and severity of adverse events
大体时间:Up to 28 days after META 10-19 infusion.
Assessed by CTCAE Version 6.0.
Up to 28 days after META 10-19 infusion.

次要结果测量

结果测量
措施说明
大体时间
Proportion of patients achieving response
大体时间:On Day 28 and at Months 2, 3, and 6 after META 10-19 infusion.
Response is assessed based on hemoglobin (Hb), laboratory markers of hemolysis (serum bilirubin and lactate dehydrogenase), and transfusion requirements.
On Day 28 and at Months 2, 3, and 6 after META 10-19 infusion.
The maximum concentration (Cmax)
大体时间:Up to 6 months after META 10-19 infusion.
The Cmax of CAR-T cell expansion in peripheral blood.
Up to 6 months after META 10-19 infusion.
Time to Peak (Tmax)
大体时间:Up to 6 months after META 10-19 infusion.
The time to reach the maximum concentration (Tmax).
Up to 6 months after META 10-19 infusion.
AUC(0-day 28)
大体时间:Up to 28 days after META 10-19 infusion.
AUC(0- day28) refers to the area under curve of CAR T-cell expansion between infusion and day 28 post infusion.
Up to 28 days after META 10-19 infusion.
Pharmacodynamics
大体时间:Up to 6 months after META 10-19 infusion.
Pharmacodynamic effects will be assessed by changes in B-cell levels in peripheral blood and bone marrow, including percentage and absolute counts of B cells and plasma cells at different time points after infusion.
Up to 6 months after META 10-19 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。

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7月8日

初级完成 (估计的)

2027年5月1日

研究完成 (估计的)

2028年10月1日

研究注册日期

首次提交

2026年6月29日

首先提交符合 QC 标准的

2026年7月6日

首次发布 (实际的)

2026年7月8日

研究记录更新

最后更新发布 (实际的)

2026年7月8日

上次提交的符合 QC 标准的更新

2026年7月6日

最后验证

2026年7月1日

更多信息

与本研究相关的术语

计划个人参与者数据 (IPD)

计划共享个人参与者数据 (IPD)?

不

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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