A Study of Rocbrutinib in Combination With Lacutoclax in Patients With B-Cell Malignancies
A Phase Ib/II, Open-Label, Multicenter Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Preliminary Efficacy of BTK Inhibitor Rocbrutinib in Combination With BCL-2 Inhibitor Lacutoclax in Patients With B-Cell Malignancies
研究概览
地位
研究类型
注册 (估计的)
阶段
- 阶段2
- 阶段1
联系人和位置
学习联系方式
- 姓名:Lugui Qiu
- 电话号码:+86-13821266636
- 邮箱:qiulg@ihcams.ac.cn
学习地点
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Tianjin、中国
- 招聘中
- Institute of Hematology & Blood Diseases Hospital, Chinese Academy of Medical Sciences
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接触:
- Lugui Qiu
- 电话号码:+86-13821266636
- 邮箱:qiulg@ihcams.ac.cn
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-
参与标准
资格标准
适合学习的年龄
- 成人
- 年长者
接受健康志愿者
描述
Inclusion Criteria:
- Age ≥18 years, regardless of sex.
Ib: Histologically confirmed diagnosis of CLL/SLL (per 2018 iwCLL criteria) or B-cell malignancies (per 2022 WHO classification), including: MCL, DLBCL, FL, and WM. Must have received at least one prior line of systemic therapy, with documented disease progression or intolerance.
II: For Treatment-naïve (TN) CLL/SLL patients: Must meet iwCLL treatment indications and no prior systemic therapy. For R/R CLL/SLL patients: at least one prior systemic therapy with documented disease progression or intolerance.
- Have at least one measurable lesion.
- Phase Ib: ECOG performance status ≤1; phase II: ECOG performance status ≤2.
- Life expectancy ≥ 12 weeks.
- Adequate coagulation function, liver and kidney function, bone marrow hematopoietic function.
- Male patients and female patients of childbearing potential must agree to use effective contraception during the study and for 90 days after the last dose of study treatment. Female patients of childbearing potential must have a negative pregnancy test before study treatment and must not be breastfeeding. Male patients must not donate sperm during the study and for 90 days after the last dose.
- Participation is voluntary, requiring signed informed consent and compliance with the treatment regimen and visit schedule.
Exclusion Criteria:
- Known hypersensitivity or intolerance to Rocbrutinib, Lacutoclax, or any of their excipients; prior treatment with any BCL-2 inhibitor; or prior treatment with both covalent and non-covalent BTK inhibitors.
- Use of systemic corticosteroids at doses equivalent to >20 mg/day of prednisone for ≥3 days within 7 days prior to the first dose.
- History of or currently suspected Richter's syndrome.
- Known or suspected central nervous system (CNS) involvement.
- Prior allogeneic hematopoietic stem cell transplantation (allo-HSCT), or autologous hematopoietic stem cell transplantation (auto-HSCT) or chimeric antigen receptor T-cell (CAR-T) therapy within 90 days before the first dose of study treatment.
- Received antitumor therapy, investigational agents, major surgery, severe trauma, or live attenuated vaccines within 4 weeks or 5 half-lives prior to the first dose of study treatment.
- Received herbal medicines for antitumor treatment, or localized radiotherapy within 14 days prior to the first dose of study treatment.
- Use of moderate or strong CYP3A inhibitors within 7 days prior to the first dose of study treatment, or consumption of grapefruit, grapefruit juice, starfruit, or Seville oranges within 3 days prior to prior to the first dose.
- History of other active malignancies within the past 3 years, except for curatively treated basal cell carcinoma, localized squamous cell carcinoma of the skin, carcinoma in situ of the cervix or breast, or other malignancies considered cured.
- Any severe and/or uncontrolled systemic disease, or any other condition that, in the opinion of the investigator, makes the patient unsuitable for participation in the study.
- Any of the following events within 6 months prior to the first dose: Symptomatic arrhythmia, myocardial infarction, intracranial hemorrhage, or Stroke.
- Impaired cardiac function.
- Any uncontrolled systemic infection.
- Conditions that may impair oral drug administration or significantly affect absorption or pharmacokinetics of the study drug.
- Unable to discontinue moderate or strong CYP3A inhibitors or inducers, P-gp (P-glycoprotein) inhibitors, sensitive substrates of OATP1B3 or CYP2C8 during the study period.
- Received vaccination with any live-attenuated vaccines within 4 weeks prior to the first dose of study treatment.
- Evidence of an active bleeding constitution or a history of significant hemorrhagic disorders.
- Requirement for ongoing therapy with warfarin or other vitamin K antagonists.
- Presence of an active, uncontrolled, or symptomatic autoimmune disease that requires systemic treatment.
- Any other condition that, in the investigator's judgment, makes the patient unsuitable for study participation.
学习计划
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:Lacutoclax+Rocbrutinib
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Phase Ib dose-escalation study of Rocbrutinib in combination with Lacutoclax. Rocbrutinib will be administered at a fixed dose of 150 mg once daily (QD), while Lacutoclax will be dose-escalated. Initial dose levels include Lacutoclax 200 mg QD and 400 mg QD in 28-day treatment cycles.Treatment will continue until disease progression, unacceptable toxicity/intolerance, or completion of the protocol-defined treatment duration, whichever occurs first. In phase II, participants will receive Rocbrutinib monotherapy for 8-12 weeks prior to combination treatment. Upon initiation of combination therapy, Lacutoclax will undergo dose ramp-up to the target dose and will then be administered continuously at the target dose. Treatment will continue until disease progression, unacceptable toxicity/intolerance, or completion of the protocol-defined treatment duration, whichever occurs first. |
研究衡量的是什么?
主要结果指标
结果测量 |
大体时间 |
|---|---|
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Phase Ib: Dose-limiting toxicity (DLT)
大体时间:At the end of Cycle 1 (the length of cycle 1 is 28 days)
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At the end of Cycle 1 (the length of cycle 1 is 28 days)
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Phase Ib: Maximum Tolerated Dose (MTD)
大体时间:At the end of Cycle 1 (the length of cycle 1 is 28 days)
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At the end of Cycle 1 (the length of cycle 1 is 28 days)
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Phase Ib: 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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Phase Ib: Time to Maximum Plasma Concentration (Tmax)
大体时间:From 1 hour prior to administration to 24 hours post-dose
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From 1 hour prior to administration to 24 hours post-dose
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Phase Ib: Maximum Plasma Concentration (Cmax)
大体时间:From 1 hour prior to administration to 24 hours post-dose
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From 1 hour prior to administration to 24 hours post-dose
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Phase Ib: Area Under the Plasma Concentration-Time Curve from Time Zero to Time t (AUC0-t)
大体时间:From 1 hour prior to administration to 24 hours post-dose
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From 1 hour prior to administration to 24 hours post-dose
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Phase Ib: Half-life (t1/2)
大体时间:From 1 hour prior to administration to 24 hours post-dose
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From 1 hour prior to administration to 24 hours post-dose
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Phase II: Undetectable minimal residual disease (uMRD) rate assessed by flow cytometry
大体时间:Up to approximately three years
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Up to approximately three years
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次要结果测量
结果测量 |
大体时间 |
|---|---|
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Phase II: Maximum Plasma Concentration (Cmax)
大体时间:From 1 hour prior to administration to 24 hours post-dose
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From 1 hour prior to administration to 24 hours post-dose
|
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Phase II: Time to Maximum Plasma Concentration (Tmax)
大体时间:From 1 hour prior to administration to 24 hours post-dose
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From 1 hour prior to administration to 24 hours post-dose
|
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Phase II: Area Under the Plasma Concentration-Time Curve from Time Zero to Time t (AUC0-t)
大体时间:From 1 hour prior to administration to 24 hours post-dose
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From 1 hour prior to administration to 24 hours post-dose
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Phase II: Half-life (t1/2)
大体时间:From 1 hour prior to administration to 24 hours post-dose
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From 1 hour prior to administration to 24 hours post-dose
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Overall Response Rate(ORR)
大体时间:Up to approximately three years
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Up to approximately three years
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Progression-free Survival(PFS)
大体时间:Up to approximately three years
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Up to approximately three years
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Overall Survival(OS)
大体时间:Up to approximately three years
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Up to approximately three years
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Phase II: 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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Complete Response Rate (CRR)
大体时间:Up to approximately three years
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Up to approximately three years
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Duration of Response (DOR)
大体时间:Up to approximately three years
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Up to approximately three years
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Phase Ib: Undetectable Minimal Residual Disease (uMRD) Rate assessed by flow cytometry
大体时间:Up to approximately three years
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Up to approximately three years
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合作者和调查者
研究记录日期
研究主要日期
学习开始 (实际的)
初级完成 (估计的)
研究完成 (估计的)
研究注册日期
首次提交
首先提交符合 QC 标准的
首次发布 (实际的)
研究记录更新
最后更新发布 (实际的)
上次提交的符合 QC 标准的更新
最后验证
更多信息
与本研究相关的术语
其他相关的 MeSH 术语
其他研究编号
- LP-10822
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研究美国 FDA 监管的设备产品
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