A Study to Evaluate the Safety and Efficacy of SCTB35 in Combination With Gemcitabine and Oxaliplatin in Patients With Relapsed or Refractory Diffuse Large B-Cell Lymphoma
2026年8月11日 更新者:Sinocelltech Ltd.
A Phase 3 Randomized, Open-label, Multicenter Study to Evaluate the Safety and Efficacy of SCTB35 in Combination With Gemcitabine and Oxaliplatin Versus Rituximab in Combination With Gemcitabine and Oxaliplatin in Patients With Relapsed or Refractory Diffuse Large B-Cell Lymphoma
The purpose of this study is to evaluate the efficacy and safety of SCTB35 in Combination With Gemcitabine and Oxaliplatin vs Rituximab in Combination With Gemcitabine and Oxaliplatin in Patients With Relapsed or Refractory Diffuse Large B-Cell Lymphoma.
研究概览
研究类型
介入性
注册 (估计的)
101
阶段
- 第三阶段
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。
学习地点
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Beijing、中国、100142
- 招聘中
- Beijing Cancer Hospital
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接触:
- Yuqin Song, M.D.
- 电话号码:010-88196118
- 邮箱:SongYQ_VIP@163.com
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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 18-80 years old
- Histologically confirmed diffuse large B-cell lymphoma according to WHO 2022 criteria
- Relapsed or refractory (R/R) disease following at least one prior systemic regimen that contained an anti-CD20 monoclonal antibody (mAb) in combination with chemotherapy
- Participants who have failed after one prior line of therapy are not candidates for high-dose chemotherapy followed by autologous stem cell transplant (ASCT)
- Presence of measurable or evaluable disease at baseline ECOG PS 0-2
- ECOG PS 0-2
- Adequate organ function and bone marrow function
- Expected survival ≥ 3 months
Exclusion Criteria:
- Prior treatment with antibodies targeting both CD20 and CD3
- Contraindication to rituximab, gemcitabine or oxaliplatin, or prior treatment with an anti-CD20 antibody in combination with the GemOx regimen
- Peripheral neuropathy assessed to be Grade >1 according to National Cancer Institute Common Terminology Criteria for Adverse Events (NCI CTCAE) v6.0 at enrollment
- Known central nervous system (CNS) involvement by lymphoma
- Known any major episode of active infection requiring treatment with systemic antibiotics within 2 weeks
- Treatment with chimeric antigen receptor T-cell (CAR-T) therapy within 100 days prior to first SCTB35 administration
- Autologous HSCT within 100 days prior to first SCTB35 administration, or any prior allogeneic HSCT or solid organ transplantation
- Major surgery within 4 weeks prior to first SCTB35 administration
- Chemotherapy and other non-investigational antineoplastic agents (except CD20 mAbs) within 4 weeks or 5 half-lives (whichever is shorter) prior to first SCTB35 administration
- Administration of a live, attenuated vaccine within 4 weeks before first study treatment administration or anticipation that such a live, attenuated vaccine will be required during the 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:随机化
- 介入模型:并行分配
- 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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有源比较器:R-GemOx
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参与者将在每个周期的第 1 天接受 IV rituxumab,最多 8 个周期。
Participants will receive IV gemcitabine administration for up to 8 cycles.
Participants will receive IV oxaliplatin administration for up to 8 cycles.
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实验性的:SCTB35-GemOx
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SCTB35 will be subcutaneously administered at a dose as specified
Participants will receive IV gemcitabine administration for up to 8 cycles.
Participants will receive IV oxaliplatin administration for up to 8 cycles.
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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 |
|---|---|---|
|
Adverse Events
大体时间:Up to approximately 3 years
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Treatment-emergent adverse events/serious adverse events/adverse events of special interest
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Up to approximately 3 years
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Progression free survival (PFS)
大体时间:Up to approximately 3 years
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Defined as the time from the date of randomization to the date of first documentation of progression disease (PD) or the date of death from any cause, whichever occurs first.
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Up to approximately 3 years
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次要结果测量
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
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Percentage of Participants Achieving Best Overall Response (BOR)
大体时间:Up to approximately 3 years
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BOR is defined as Complete Response (CR) or Partial Response (PR), determined by Lugano criteria
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Up to approximately 3 years
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Percentage of Participants Achieving CR
大体时间:Up to approximately 3 years
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Percentage of participants who achieve a CR determined per Lugano criteria.
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Up to approximately 3 years
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Overall Survival (OS)
大体时间:Up to approximately 3 years
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Overall survival is defined as the duration from the date of randomization to the date of the participant's death.
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Up to approximately 3 years
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Duration of Response (DOR)
大体时间:Up to approximately 3 years
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DOR is defined as the time from the first occurrence of response (CR or PR) to disease progression or death, whichever occurs first.
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Up to approximately 3 years
|
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Time to Response (TTR)
大体时间:Up to approximately 3 years
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Time to response is defined for participants achieving a CR/PR as the time from starting therapy to first a CR/PR.
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Up to approximately 3 years
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Event-Free Survival (EFS)
大体时间:Up to approximately 3 years
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EFS is defined as the duration from randomization to disease progression determined by Lugano criteria as assessed by the investigator, initiation of any non-protocol-specified new anti-lymphoma therapy for any reason, or death (whichever occurs first).
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Up to approximately 3 years
|
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Duration of Complete Response (DOCR)
大体时间:Up to approximately 3 years
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DOCR is defined as the time from the first occurrence of CR to disease progression or death, whichever occurs first.
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Up to approximately 3 years
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Time to Complete Response (TTCR)
大体时间:Up to approximately 3 years
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Time to complete response is defined for participants achieving a CR as the time from starting therapy to first a CR.
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Up to approximately 3 years
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Blood Concentrations of SCTB35
大体时间:Up to approximately 1 years
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The pharmacokinetics of SCTB35 will be analyzed based on the drug concentrations at respective timepoints in the blood samples (or blood derivative)
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Up to approximately 1 years
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Anti-drug Antibodies of SCTB35
大体时间:Up to approximately 3 years
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Blood samples (or blood derivative) will be screened for antibodies binding to SCTB35
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Up to approximately 3 years
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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。
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 (实际的)
2026年6月4日
初级完成 (估计的)
2027年11月1日
研究完成 (估计的)
2029年4月1日
研究注册日期
首次提交
2026年4月29日
首先提交符合 QC 标准的
2026年4月29日
首次发布 (实际的)
2026年5月6日
研究记录更新
最后更新发布 (实际的)
2026年8月13日
上次提交的符合 QC 标准的更新
2026年8月11日
最后验证
2026年8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.