CD20 Monoclonal Antibody Combined With BTK Inhibitor for the Treatment of Refractory Immune-related Cytopenia
2026年5月19日 更新者:Qi deng
Clinical Study on the Treatment of Refractory Immune-related Cytopenia With CD20 Monoclonal Antibody Combined With BTK Inhibitor (BTKi)
This study aims to utilize anti-CD20 monoclonal antibodies to eliminate peripheral B cells and reduce the mechanism of autoantibody production, as well as combine the mechanism of BTK inhibitors (BTKi) blocking the B cell receptor signaling pathway and inhibiting B cell activation and proliferation, for the treatment of refractory immune-related cytopenia.
In this study, it includes the salvage treatment of immune thrombocytopenia (ITP) and autoimmune hemolytic anemia (AIHA), expecting to achieve a synergistic and enhancing effect.
This study aims to select Zuberitamab, a human-mouse chimeric anti-CD20 monoclonal antibody, and the BTKi Orelabrutinib as combination therapy options.
The clinical efficacy of the Zuberitamab-Orelabrutinib combination therapy (overall response rate, duration of sustained remission) will be evaluated, along with its safety profile (including infections, bleeding, cardiac toxicity), to provide a theoretical basis for their combined use in treating refractory immune-related thrombocytopenia (ITP and AIHA).
研究概览
地位
尚未招聘
研究类型
介入性
注册 (估计的)
30
阶段
- 阶段1
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:
- Diagnosed with refractory immune-related cytopenia, including immune thrombocytopenic purpura (ITP) and autoimmune hemolytic anemia (AIHA);
- Age ranging from 18 to 80 years old (inclusive of 18 and 80);
- Expected survival time > 12 months;
Good function of major organs:
- liver function: ALT/AST < 3 times the upper limit of normal;
- kidney function: creatinine < 100 μmol/L;
- lung function: indoor oxygen saturation ≥ 95%;
- heart function: left ventricular ejection fraction (LVEF) ≥ 50%;
- Peripheral superficial venous blood flow is unobstructed, capable of meeting the requirements for intravenous infusion;
- Karnofsky score ≥ 60, ECOG ≤ 2 points.
Exclusion Criteria:
- Women who are pregnant (with positive urine/blood pregnancy test results) or breastfeeding;
Those who have severe underlying heart diseases when participating in this study, including:
- clinically significant atrial fibrillation (AF),
- cardiac conduction block,
- myocardial infarction (within 1 year),
- congestive heart failure (CHF);
- cardiac echocardiography LVEF < 50%;
- New York Heart Association (NYHA) cardiac function classification of III-IV grade;
- Those with active bleeding or bleeding tendencies, and those who need to take anticoagulant drugs;
- Those with organ dysfunction or uncontrollable coexisting diseases;
- History of malignant tumors;
- Those with active chronic hepatitis B or active hepatitis C;
- Known history of human immunodeficiency virus (HIV) infection and/or acquired immunodeficiency syndrome;
- Those with uncontrollable infectious diseases;
- As determined by the investigator, other unsuitable conditions exist.
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 |
|---|---|
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实验性的:Zuberitamab-Orelabrutinib combination therapy
This study is designed as a non-randomized, single-arm, open-label clinical trial.
Patients with refractory immune-related cytopenia, including immune thrombocytopenia (ITP) and autoimmune hemolytic anemia (AIHA), are intended for enrollment.
The treatment regimen and schedule are as follows: anti-CD20 monoclonal antibody (Zuberitamab): 100 mg per dose on Days 1, 8, 15, and 22; BTK inhibitor (Orelabrutinib): 50 mg once daily (qd) from Day 1 to Day 90.
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This is a novel combination regimen of anti-CD20 monoclonal antibody plus BTKi, specifically designed for patients with refractory immune-related cytopenia.
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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 |
|---|---|---|
|
Evaluate the Median overall response rate at 6 months of anti-CD20 monoclonal antibody and BTKi combination therapy in refractory immune-related cytopenia
大体时间:Six month after treatment initiation
|
Median overall response rate at 6 months after treatment initiation
|
Six month after treatment initiation
|
次要结果测量
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
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Evaluate the early overall response rate 3 months after the start of anti-CD20 monoclonal antibody and BTKi combination therapy in refractory immune-related cytopenia
大体时间:Three month after therapy
|
The early overall response rate 3 months after the start of treatment
|
Three month after therapy
|
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Evaluate the sustained remission rate that lasts for 6 months after achieving remission following anti-CD20 monoclonal antibody and BTKi combination therapy in refractory immune-related cytopenia
大体时间:Six month after achieving remission
|
The sustained remission rate that lasts for 6 months after achieving remission
|
Six month after achieving remission
|
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Evaluate the Incidence of Treatment-Emergent Adverse Events (Safety and Tolerability) of anti-CD20 monoclonal antibody and BTKi combination therapy in refractory immune-related cytopenia
大体时间:Up to three month after therapy
|
The incidence and severity of therapy related toxic reactions (including infections, bleeding, cardiac toxicity)
|
Up to three month after therapy
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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。
赞助
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1日
初级完成 (估计的)
2028年5月31日
研究完成 (估计的)
2028年5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1日
首次发布 (实际的)
2026年5月7日
研究记录更新
最后更新发布 (实际的)
2026年5月22日
上次提交的符合 QC 标准的更新
2026年5月19日
最后验证
2026年5月1日
更多信息
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.