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IASO206 in Patients With Relapsed/Refractory Autoimmune Hemolytic Anemia

2026年5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 IASO206 Injection in Patients With Relapsed/Refractory Autoimmune Hemolytic Anemia

This study is an open-label, single-arm early exploratory clinical study, aiming to evaluate the safety, tolerability and preliminary efficacy of IASO206 Injection (In Vivo CAR-T) in Patients with Relapsed/Refractory Autoimmune Hemolytic Anemia

研究概览

研究类型

介入性

注册 (估计的)

18

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

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:

  • Age 18 to 75 years, gender unrestricted.
  • Diagnosis of AIHA (including warm antibody type, warm-cold antibody type, cold agglutinin disease) or Evans syndrome, consistent with Chinese Expert Consensus on Diagnosis and Treatment of Autoimmune Hemolytic Anemia (2023), 2019 International Consensus for Diagnosis and Management of Autoimmune Hemolytic Anemia (Blood Rev, 2020), or Chinese Expert Consensus on Diagnosis and Treatment of Evans Syndrome (2024 Edition).
  • Patients with relapsed/refractory disease after multiple lines of therapy must meet all of the following criteria: hemoglobin < 10 g/dL with clinical manifestations of hemolytic anemia; prior treatment with at least 2 immunosuppressive drugs (must include CD20 monoclonal antibody); glucocorticoid therapy for at least 3 months (excluded are patients with contraindications to glucocorticoids, severe infection, severe osteoporosis, previous fracture, or inability to tolerate glucocorticoids); cumulative dose of CD20 monoclonal antibody at least 375 mg/m² × 4, or total dose 2.0 g, or at least 6 administrations (at least 1 week apart each time).
  • ECOG score ≤ 2.
  • Expected survival time ≥ 12 weeks.
  • Adequate organ function confirmed by laboratory tests: serum alanine aminotransferase (ALT) and aspartate aminotransferase (AST) ≤ 1.5 × upper limit of normal (ULN); minimum pulmonary reserve defined as grade ≤ 1 dyspnea and oxygen saturation ≥ 93% without oxygen supplementation; creatinine clearance (estimated by Cockcroft-Gault) ≥ 45 mL/min; cardiac ejection fraction ≥ 50%, no pericardial effusion on echocardiogram (ECHO), and no clinically significant abnormal electrocardiogram (ECG).
  • Subjects and their partners agree to use effective barrier or medical contraceptive measures (excluding rhythm method) from signing informed consent until 1 year after administration.
  • Subjects must provide written informed consent approved by the Ethics Committee prior to initiation of screening procedures

Exclusion Criteria:

  • Subject with confirmed lymphoproliferative neoplasms.
  • Subject with secondary AIHA induced by drugs or infection.
  • Subject with congenital immunodeficiency diseases, other hereditary or acquired hemolytic diseases.
  • Subject with a history of organ or stem cell transplantation.
  • Subject with a history of organ infarction within the past 6 months.
  • Subject who have received prior BCMA-targeted therapy.
  • Subject who received plasma cell-targeted cell therapy within 3 months before screening, or in whom prior cell therapy products are still detectable in peripheral blood.
  • Subject who received any of the following treatments within the specified periods prior to study enrollment:

    1. Anti-CD20 monoclonal antibody < 12 weeks;
    2. Sutimlimab or other marketed biological products < 5 half-lives;
    3. Plasma exchange < 4 weeks;
    4. Splenectomy < 12 weeks.
  • Subject with any of the following cardiovascular diseases:

    1. Left ventricular ejection fraction (LVEF) ≤ 45%;
    2. Active heart disease or congestive heart failure (New York Heart Association [NYHA] Class III or IV);
    3. Severe arrhythmia requiring treatment (excluding atrial fibrillation, paroxysmal supraventricular tachycardia);
    4. QTcB interval ≥ 450 ms for males, ≥ 470 ms for females;
    5. Myocardial infarction, bypass surgery, or stent implantation within 6 months before study;
    6. Other cardiac diseases judged by the investigator to be unsuitable for enrollment.
  • Unstable systemic diseases judged by the investigator, including but not limited to severe hepatic or renal diseases requiring medical treatment.
  • Subject with a history of other primary malignancies within 5 years before screening, except:

    1. Resected and cured non-melanoma skin cancer (e.g., basal cell carcinoma);
    2. Cured carcinoma in situ (e.g., cervical, bladder, or breast cancer);
    3. Other primary cancers with no evidence of recurrence for more than 5 years after treatment.
  • Subject who underwent major surgery within 4 weeks before screening and are judged unsuitable for enrollment by the investigator.
  • Subject with uncontrolled active fungal, viral, bacterial, mycobacterial, or other infections (persistent infection-related signs/symptoms without improvement after appropriate anti-infective therapy) or infections requiring intravenous anti-infective therapy.
  • Positive hepatitis B surface antigen (HBs-Ag) or hepatitis B e antigen (HBe-Ag); positive hepatitis B e antibody (HBe-Ab) or hepatitis B core antibody (HBc-Ab) with HBV-DNA copy number above the lower limit of quantification; positive hepatitis C (HCV) antibody; positive human immunodeficiency virus (HIV) antibody; active syphilis infection (excluding those with only positive syphilis-specific antibody).
  • Subject who received live viral vaccines within 4 weeks before enrollment.
  • Subject who are participating in other interventional clinical studies during IASO206 Injection treatment with a drug half-life < 5; subject receiving active investigational drugs during the entire study period, or who intend to participate in another clinical trial, or receive treatments outside the protocol.
  • Pregnant or lactating females.
  • Subject with psychiatric disorders, disturbance of consciousness, or central nervous system diseases, including but not limited to epilepsy and Parkinson's disease.
  • Subject with hypersensitivity to components of IASO206 Injection or supportive medications required for the management of CAR-T therapy-related toxicities (e.g., tocilizumab).
  • Other conditions judged by the investigator to be unsuitable for enrollment.10. Other Information

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:IASO206
Subjects will receive a single infusion of IASO206 injection in a 3+3 dose-escalation design. Three ascending dose cohorts are planned: 1E8 TU, 3E8 TU, and 5E8 TU. In each dose cohort, the first subject will be observed for at least 3 weeks after infusion before subsequent subjects in the same cohort receive IASO206 injection.
The third-generation self-inactivating lentiviral vector that carries a BCMA-targeted CAR. Administered in one infusion.

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 3 months after IASO206 infusion
Assessed by CTCAE Version 5.0.
Up to 3 months after IASO206 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:At Weeks 4, 8, and 12, and Months 4, 5, and 6 after IASO206 infusion
Response assessment is primarily assessed based on hemoglobin, and should be performed after discontinuation of glucocorticoids or other immunosuppressive therapies for at least 2 weeks.
At Weeks 4, 8, and 12, and Months 4, 5, and 6 after IASO206 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6月15日

初级完成 (估计的)

2026年12月31日

研究完成 (估计的)

2028年12月31日

研究注册日期

首次提交

2026年5月6日

首先提交符合 QC 标准的

2026年5月6日

首次发布 (实际的)

2026年5月13日

研究记录更新

最后更新发布 (实际的)

2026年5月13日

上次提交的符合 QC 标准的更新

2026年5月6日

最后验证

2026年5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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