Phase Ib/II Clinical Study of QLS5133 Combination Therapy in Advanced Solid Tumors
A Phase Ib/II Clinical Study on the Safety, Tolerability, Pharmacokinetics, and Efficacy of Intravenous QLS5133 Combination Therapy in Participants With Advanced Solid Tumors
The goal of this clinical trial is to evaluate the safety, tolerability, pharmacokinetics (PK), and effectiveness of the investigational drug QLS5133 (injectable) in combination with other therapies for participants with advanced solid tumors. This is a multicenter, open-label study consisting of two parts: dose escalation and tumor-specific expansion.
The main questions it aims to answer are:
- In the dose-escalation part: What is the safety, tolerability, PK profile, and preliminary efficacy of QLS5133 combination therapy, and what are the recommended dose(s) for expansion?
- In the expansion part: What is the anti-tumor efficacy and further safety profile of QLS5133 combination therapy at the selected dose(s) in participants with specific tumor types?
Participants will:
- Be enrolled in sequential cohorts to receive QLS5133 in combination with other anticancer agents.
- Undergo regular assessments for safety, drug concentration levels (PK), and tumor response.
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:Jinming Yu, PhD
- 电话号码:0531-67626073
- 邮箱:sdyujinming@126.com
学习地点
-
-
Shandong
-
Jinan、Shandong、中国、250000
- Cancer Hospital of Shandong First Medical University
-
-
参与标准
资格标准
适合学习的年龄
接受健康志愿者
有资格学习的性别
描述
Inclusion Criteria:
- 1. Histologically or cytologically confirmed advanced solid tumors, with specific tumor type and prior treatment requirements per each cohort;
- 2. Measurable disease per RECIST v1.1 (except Cohorts 3B-1, 3B-2, and 5B);
- 3.Eastern Cooperative Oncology Group (ECOG) performance status 0-1;
- 4.Adequate organ function;
- 5.Recover from all reversible AEs from previous anti-tumor treatment (i.e., Grade ≤ 1, according to NCI-CTCAE v6.0), excluding alopecia (any grade) and Grade ≤ 2 neuropathy peripheral;.
Exclusion Criteria:
- 1.Prior treatment with CDH6-targeted agents or topoisomerase I inhibitors (including ADCs);
- 2.Prior treatment with immune checkpoint inhibitors (for Cohorts 2 and 6 only);
- 3.Prior Grade 4 or persistent ≥ 4-week Grade 3 immune-related AEs from immune checkpoint inhibitors;
- 4.Prior systemic anti-tumor therapy (for Cohorts 1B-2 and 2B-2 only);
- 5.Recent anti-tumor therapy within specified washout periods (small molecules: 2 weeks; biologics/chemotherapy: 4 weeks; mitomycin/nitrosoureas: 6 weeks);
- 6.Active or symptomatic CNS metastases or leptomeningeal carcinomatosis;
- 7. Serious, uncontrolled medical disorder, nonmalignant systemic disease, or active, uncontrolled infection;
- 8.History of significant cardiac disease, or poorly controlled diabetes mellitus;
- 9.History of recurrent autoimmune diseases;
- 10. History of a second primary malignancy;
- 11.Be allergic to any component of QLS5133 or its excipients.
学习计划
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: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 |
|---|---|
|
实验性的:Arm 1
QLS5133 in combination with lenvatinib mesylate |
QLS5133: Intravenous infusion, Q3W; Lenvatinib mesylate: Oral, once daily |
|
实验性的:Arm 2
QLS5133 in combination with lenvatinib mesylate plus QL2107 |
QLS5133 and QL2107: Intravenous infusion, Q3W; Lenvatinib mesylate: Oral, once daily |
|
实验性的:Arm 3
QLS5133 in combination with bevacizumab |
Intravenous infusion,Q3W |
|
实验性的:Arm 4
QLS5133 in combination with platinum-based therapy with or without bevacizumab, followed by QLS5133 alone or in combination with bevacizumab |
Intravenous infusion,Q3W |
|
实验性的:Arm 5
QLS5133 in combination with olaparib with or without bevacizumab |
Olaparib is oral; all others are intravenous infusion,Q3W |
|
实验性的:Arm 6
QLS5133 in combination with QL2107 with or without bevacizumab |
Intravenous infusion,Q3W |
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 |
|---|---|---|
|
Phase Ib Outcome 1:Incidence and severity of adverse events and serious adverse events
大体时间:up to 2 years
|
Incidence and severity of adverse events, serious adverse events, according to NCI-CTCAE Version 6.0 |
up to 2 years
|
|
Phase Ib Outcome 2:Maximum tolerated dose (MTD)
大体时间:28 days
|
Highest administered dose with < 33% participants experiencing dose limiting toxicity (DLT) in the first 6 DLT evaluable participants |
28 days
|
|
Phase Ib Outcome 3:Recommended Phase 2 Dose (RP2D)
大体时间:up to 2 years
|
Based on the maximum tolerated dose, cumulative safety, and pharmacokinetic data |
up to 2 years
|
|
Phase II outcome 1:Objective response rate (ORR) (Arms 1B, 2B, 3B-3, 4B, 6B)
大体时间:up to 2 years
|
ORR is defined as the percentage of participants achieved complete response or partial response as assessed according to RECIST v1.1 criteria. |
up to 2 years
|
|
Phase II outcome 2:Progression-free survival (PFS) (Arms 3B-1, 3B-2, and 5B)
大体时间:up to 2 years
|
PFS is defined as the duration from the date of first dose of study treatment to the date of first documented PD per investigator assessment, or death from any cause, whichever occurs first. |
up to 2 years
|
合作者和调查者
研究记录日期
研究主要日期
学习开始 (估计的)
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
- QLS5133-201
计划个人参与者数据 (IPD)
计划共享个人参与者数据 (IPD)?
药物和器械信息、研究文件
研究美国 FDA 监管的药品
研究美国 FDA 监管的设备产品
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