A Study of Rocbrutinib Combined With R-GemOx in Patients With Relapsed or Refractory Diffuse Large B-cell Lymphoma
2026年9月9日 更新者:Guangzhou Lupeng Pharmaceutical Company LTD.
A Phase Ib Study to Evaluate the Safety and Efficacy of Rocbrutinib in Combination With Rituximab, Gemcitabine, Oxaliplatin (R-GemOx) in Patients With Refractory or Relapsed Diffuse Large B-cell Lymphoma
This is a multicenter, open-label phase Ib study, evaluating the safety, tolerability, preliminary efficacy and PK characteristics of Rocbrutinib (LP-168) combined with R-GemOx in patients with R/R non-GCB DLBCL.
Study includes dose escalation part and dose expansion part.
In the dose escalation part, a classic "3+3" design will be used to assess the safety of each specified dose combination.
Upon completion of a predefined escalation part, the decision on whether to proceed to the dose expansion part will be based on the safety, PK, and efficacy data of the combination regimen.
研究概览
研究类型
介入性
注册 (估计的)
42
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
- 姓名:Qingqing Cai
- 电话号码:086-20-87343355
- 邮箱:caiqq@sysucc.org.cn
研究联系人备份
- 姓名:Rong Tao
- 电话号码:086-210-64175590
- 邮箱:hkutao@hotmail.com
学习地点
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Guangdong
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Guangzhou、Guangdong、中国、510050
- 招聘中
- Sun Yat-sen University Cancer Center
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接触:
- Qingqing Cai
- 电话号码:086-20-87343355
- 邮箱:caiqq@sysucc.org.cn
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Shanghai Municipality
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Shanghai、Shanghai Municipality、中国、200032
- 招聘中
- Fudan University Shanghai Cancer Center
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接触:
- Rong Tao
- 电话号码:086-210-64175590
- 邮箱:hkutao@hotmail.com
-
-
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:
- Patients with relapsed or refractory non-GCB DLBCL.
- Have at least one measurable lesion according to the Lugano Response Criteria 2014.
- ECOG performance status 0-2 (0-1 for dose escalation part).
- Life expectancy ≥ 12 weeks.
- Adequate coagulation function, liver and kidney function, bone marrow hematopoietic function.
- No plan for autologous/allogeneic hematopoietic stem cell transplantation or chimeric antigen receptor T-cell (CAR-T) therapy.
- Toxicities from prior anti-tumor therapy have recovered to Grade ≤1 according to NCI CTCAE v5.0.
- All male subjects and female subjects of childbearing potential must strictly use medically approved contraception throughout the entire study period. All male subjects must also avoid sperm donation during the above period. For women of childbearing potential, the result of serum pregnancy test must be obtained. Women must be non-lactating
- Subjects must provide adequate tissue and blood samples for exploratory study. Participation is voluntary, requiring signed informed consent and compliance with the treatment regimen and visit schedule.
Exclusion Criteria:
- Intolerance to Rocbrutinib or any drug in the combination regimen.
- Prior treatment with a BTK-targeted therapy; prior treatment with R-GemOx.
- DLBCL transformed from an indolent lymphoma; diagnosis of high-grade or double-hit DLBCL.
- Chemotherapy, biologic therapy (except CAR-T), immunotherapy or major surgery within 4 weeks of the first dose of study treatment.
- Small molecule targeted therapy within 4 weeks or within 5 half-lives (whichever is shorter) of the first dose of study treatment.
- Herbal or proprietary Chinese medicines with antitumor activity or radiotherapy with a limited field of radiation within 7 days of the first dose of study treatment.
- History of allogeneic hematopoietic stem-cell transplantation (allo-HSCT) or other organ transplantation, or autologous HSCT (auto-HSCT) or chimeric antigen receptor T-cell (CAR-T) therapy within 90 days of the first dose of study treatment.
- Current corticosteroid therapy at a dose >20 mg/day prednisone equivalent. The prednisone-equivalent dose must have been stable for at least 4 weeks before Cycle 1 Day 1.
- Unable to discontinue prohibited medications during the study period (strong or moderate CYP3A inhibitors or inducers, P-gp inhibitors, OATP1B3-sensitive substrates, warfarin or other vitamin K antagonists).
- Known or suspected CNS involvement by lymphoma.
- Presence of peripheral neuropathy > Grade 1.
- Any severe and/or uncontrolled systemic disease, or condition affecting drug swallowing or absorption, that in the investigator's judgment makes the subject unsuitable for 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:非随机化
- 介入模型:顺序分配
- 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:Dose Level 1
Patients will receive Rocbrutinib at 150 mg once daily in combination with R-GemOx
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Patients will receive Rocbrutinib until disease progression or unacceptable toxicity
其他名称:
Patients will receive 6 cycles every 21 days of R-GemOx.
Rituximab 375mg/m2 i.v. on day 1 of every cycle.
GemOx (gemcitabine 1000mg/m2 plus oxaliplatin 100mg/m2) i.v. on day 2 of each cycle.
|
|
实验性的:Dose Level 2
Patients will receive Rocbrutinib at 200 mg once daily in combination with R-GemOx
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Patients will receive Rocbrutinib until disease progression or unacceptable toxicity
其他名称:
Patients will receive 6 cycles every 21 days of R-GemOx.
Rituximab 375mg/m2 i.v. on day 1 of every cycle.
GemOx (gemcitabine 1000mg/m2 plus oxaliplatin 100mg/m2) i.v. on day 2 of each cycle.
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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 |
|---|---|---|
|
DLTs
大体时间:At the end of Cycle 1 (the length of cycle 1 is 21 days)
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Dose-Limiting Toxicities
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At the end of Cycle 1 (the length of cycle 1 is 21 days)
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MTD
大体时间:At the end of Cycle 1 (the length of cycle 1 is 21 days)
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Maximum Tolerated Dose
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At the end of Cycle 1 (the length of cycle 1 is 21 days)
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Adverse events as assessed by CTCAE v5.0
大体时间:From the first administration to 28 days after the last administration
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From the first administration to 28 days after the last administration
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次要结果测量
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
|
ORR
大体时间:Up to approximately two years
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Overall Response Rate
|
Up to approximately two years
|
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TTR
大体时间:Up to approximately two years
|
Time to Response
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Up to approximately two years
|
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DoR
大体时间:Up to approximately two years
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Duration of Response
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Up to approximately two years
|
|
PFS
大体时间:Up to approximately two years
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Progression-free Survival
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Up to approximately two years
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OS
大体时间:Up to approximately two years
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Overall Survival
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Up to approximately two years
|
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Cmax
大体时间:From 1 hour prior to administration to 24 hours post-dose
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Maximum Plasma Concentration
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From 1 hour prior to administration to 24 hours post-dose
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Tmax
大体时间:From 1 hour prior to administration to 24 hours post-dose
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Time to Maximum Plasma Concentration
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From 1 hour prior to administration to 24 hours post-dose
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AUC0-t
大体时间:From 1 hour prior to administration to 24 hours post-dose
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Area Under the Plasma Concentration-Time Curve from Time Zero to Time t
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From 1 hour prior to administration to 24 hours post-dose
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t1/2
大体时间:From 1 hour prior to administration to 24 hours post-dose
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Half-life
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From 1 hour prior to administration to 24 hours post-dose
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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25日
初级完成 (估计的)
2027年12月31日
研究完成 (估计的)
2028年7月31日
研究注册日期
首次提交
2026年4月22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9月10日
上次提交的符合 QC 标准的更新
2026年9月9日
最后验证
2026年9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.