A Study of Lacutoclax (LP-108) in Patients With Relapsed/Refractory CLL/SLL
2026年7月29日 更新者:Guangzhou Lupeng Pharmaceutical Company LTD.
A Phase 2, Open-Label, Single-Arm, Multicenter Study to Evaluate the Efficacy and Safety of Lacutoclax (LP-108) in Patients With Relapsed or Refractory Chronic Lymphocytic Leukemia/Small Lymphocytic Lymphoma
The goal of this clinical trial is to evaluate the efficacy and safety of Lacutoclax, an oral selective BCL-2 inhibitor, in patients with relapsed or refractory chronic lymphocytic leukemia/small lymphocytic lymphoma (CLL/SLL).
Lacutoclax is a potent and selective BCL-2 inhibitor with relatively weaker inhibitory activity against BCL-XL and BCL-W.
Preliminary clinical data have demonstrated promising efficacy and an acceptable safety profile in patients with CLL/SLL and other B-cell non-Hodgkin lymphomas (B-NHLs).
This is an open-label, single-arm, multicenter Phase II study evaluating the efficacy and safety of oral Lacutoclax tablets in patients with relapsed or refractory CLL/SLL.
研究概览
研究类型
介入性
注册 (估计的)
75
阶段
- 阶段2
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:Jianyong Li
- 电话号码:025-83781120
- 邮箱:lijianyonglm@126.com
学习地点
-
-
Jiangsu
-
Nanjing、Jiangsu、中国
- 招聘中
- The First Affiliated Hospital of Nanjing Medical University
-
接触:
- Huayuan Zhu
- 电话号码:86-13813810650
- 邮箱:huayuan.zhu@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 confirmed R/R CLL/SLL according to the 2018 International Workshop on Chronic Lymphocytic Leukemia (iwCLL) criteria.
- Patients who had previously received standard therapy, experienced disease progression following the most recent line of treatment (excluding intolerance), and had at least one indication for treatment prior to enrollment.
- Have at least one measurable lesion.
- Age ≥18 years, regardless of sex.
- Eastern Cooperative Oncology Group (ECOG) performance status score ≤2.
- Life expectancy ≥ 12 weeks.
- Adequate coagulation function, liver and kidney function, bone marrow hematopoietic function.
- Toxicities from prior anti-tumor therapy have recovered to Grade ≤1 according to NCI CTCAE v5.0.
- 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 Lacutoclax. 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 of Lacutoclax.
- Participation is voluntary, requiring signed informed consent and compliance with the treatment regimen and visit schedule.
Exclusion Criteria:
- Known hypersensitivity to Lacutoclax or any of its excipients.
- Prior treatment with a BCL-2 family inhibitor.
- 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 corticosteroids for antitumor purposes, 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 dosing.
- Prior malignancy other than CLL/SLL within the past 2 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.
- Major cardiovascular or cerebrovascular events within 6 months prior to the first dose of study treatment.
- Presence of any severe and/or uncontrolled systemic disease.
- 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, or sensitive CYP2C8 substrates during the study period.
- Primary autoimmune disease requiring immunosuppressive therapy.
- Any other condition that, in the investigator's judgment, makes the patient unsuitable for study participation.
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:Lacutoclax
All participants will receive oral Lacutoclax tablets once daily with dose escalation to a target dose of 400 mg.
|
Participants will first undergo a dose ramp-up period of at least 4 days (Cycle 0: C0D1-C0D4), followed by continuous administration at the target dose of 400 mg once daily starting from Cycle 1.
Each treatment cycle will last 28 days.
Treatment will continue until disease progression, unacceptable toxicity, or fulfillment of other criteria for treatment discontinuation.
|
研究衡量的是什么?
主要结果指标
结果测量 |
大体时间 |
|---|---|
|
Overall Response Rate (ORR) assessed by Independent Review Committee (IRC)
大体时间:Up to approximately 28 months
|
Up to approximately 28 months
|
次要结果测量
结果测量 |
大体时间 |
|---|---|
|
ORR assessed by Investigator(INV)
大体时间:Up to approximately 28 months
|
Up to approximately 28 months
|
|
Complete response(CR) plus complete response with incomplete bone marrow recovery (CRi) rate (CRi applicable only to patients with CLL) assessed by IRC and INV, respectively
大体时间:Up to approximately 28 months
|
Up to approximately 28 months
|
|
Time to response (TTR) assessed by IRC and INV, respectively
大体时间:Up to approximately 30 months
|
Up to approximately 30 months
|
|
Duration of response (DOR) assessed by IRC and INV, respectively
大体时间:Up to approximately 30 months.
|
Up to approximately 30 months.
|
|
Time to first 50% reduction in absolute lymphocyte count (ALC) or normalization of ALC
大体时间:Up to approximately 28 months
|
Up to approximately 28 months
|
|
Progression-free survival (PFS) assessed by IRC and INV, respectively
大体时间:Up to approximately 30 months
|
Up to approximately 30 months
|
|
Overall Survival
大体时间:Up to approximately 30 months
|
Up to approximately 30 months
|
|
Adverse events(AEs) as assessed by CTCAE v5.0
大体时间:Up to approximately 30 months
|
Up to approximately 30 months
|
|
Adverse drug reactions (ADRs) related to Lacutoclax
大体时间:Up to approximately 30 months
|
Up to approximately 30 months
|
|
Serious adverse events (SAEs)
大体时间:Up to approximately 30 months
|
Up to approximately 30 months
|
|
Maximum Plasma Concentration(Cmax)
大体时间:From 1 hour prior to administration to 24 hours post-dose
|
From 1 hour prior to administration to 24 hours post-dose
|
|
Time to Maximum Plasma Concentration (Tmax)
大体时间:From 1 hour prior to administration to 24 hours post-dose
|
From 1 hour prior to administration to 24 hours post-dose
|
|
Half-life (T1/2)
大体时间:From 1 hour prior to administration to 24 hours post-dose
|
From 1 hour prior to administration to 24 hours post-dose
|
|
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
|
From 1 hour prior to administration to 24 hours post-dose
|
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7月14日
初级完成 (估计的)
2028年3月30日
研究完成 (估计的)
2029年9月30日
研究注册日期
首次提交
2026年5月20日
首先提交符合 QC 标准的
2026年5月20日
首次发布 (实际的)
2026年5月27日
研究记录更新
最后更新发布 (实际的)
2026年7月30日
上次提交的符合 QC 标准的更新
2026年7月29日
最后验证
2026年7月1日
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-10821
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.