A Study of SHR6390 in Advanced Solid Tumor Patients
2022年7月7日 更新者:Jiangsu HengRui Medicine Co., Ltd.
A Tolerability and Pharmacokinetics Study of SHR6390 in Advanced Solid Tumor Patients
SHR6390 is a small molecular, oral potent, selective CDK4/6 inhibitor.
The purpose of this study is to investigate the safety/tolerability and the pharmacokinetic profile of SHR6390 in Chinese advanced solid tumor patients by using a "3+3" dose escalation.Preliminary efficacy will be also investigated in this study.
研究概览
研究类型
介入性
注册 (实际的)
40
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。
学习地点
-
-
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Beijing、中国
- Cancer Hospital, Chinese Academy of Medical Sciences
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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
18年 至 65年 (成人、年长者)
接受健康志愿者
不
有资格学习的性别
全部
描述
Inclusion Criteria:
- Pathologically confirmed solid tumor and failed from all standard treatment
- Eastern Cooperative Oncology Group (ECOG) performance status: 0-1
- Life expectancy ≥ 3 months
Adequate function of major organs, meaning the following criteria should be met within 14 days before randomization:
- Hemoglobin > 110g/L
- Neutrophils > 2.0×10^9/L
- Platelets > 100×10^9/L
- Total bilirubin < 1.5×the upper limit of normal (ULN)
- ALT and AST ≤ 1.5×ULN (≤ 5×ULN, if existing liver metastases)
- Creatinine ≤ 1 ULN
- Left ventricular ejection fraction (LVEF) ≥ 50%
- QTcF(Fridericia correction) male≤450 ms, female≤470 ms
- Good compliance of patient by physician's judgement
- Signed and dated informed consent
Exclusion Criteria:
- Previously received therapy of anti-tumor agent targeting at CDK4/6
- Less than 3 weeks from the last cell-toxicity chemotherapy, less than 6 weeks from last mitomycin or nitrosamine therapy
- Less than 3 weeks from any other anti-tumor therapy (including targets therapy, immunotherapy or other approved therapy)
- Having joined in other clinical trials within 4 weeks
- Uncontrolled/untreated brain metastasis (well-controlled/well-treated brain metastasis by physician's judgement is allowed)
- existing abnormal CTCAE≥grade 2 resulted from previous treatment(except grade 2 alopecia)
- uncontrollable symptomatic pleural effusion or ascites or require clinical intervention
- require continous treatment by steroids
- Factors influencing the usage of oral administration (e.g. unable to swallow, chronic diarrhea and intestinal obstruction, etc.)
- existing uncontrollable hypokalemia or hypomagnesemia
- history of serious allergy events or known being allergy constitution
- active HBV or HCV infection (HBV virus≥10e4 copies/ml, HCV virus≥10e3 copies/ml)
- History of immunodeficiency, acquired or congenital immunodeficiency, history of organ transplantation
- history of cardiac dysfunction, include(1)angina (2)clinical significant arrythmia or require drug intervention (3)myocardial infarction (4)heart failure (5) other cardiac dysfunction (judged by the physician); any cardiac or nephric abnormal ≥grade 2 found in screening
- Female patients who are pregnancy, lactation or women who are of childbearing potential tested positive in baseline pregnancy test childbearing female who refuse to accept any contraception practice
- determined by the physician, any coexisting disease might lead to life threatening complications or avoid the patients from accomplishing the treatment(e.g serious hypertension, diabetes, thyroid dysfunction,etc.)
- history of neuropathy or dysphrenia, including epilepsy and dementia
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 |
|---|---|
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实验性的:SHR6390
Each subject will receive a single dose of SHR6390 and then repeat doses following a 3 week/1 week off regimen
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SHR6390 either 25, 50mg, 75mg, 100mg, 125mg, 150mg, 175mg given orally, QD
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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 |
|---|---|---|
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Maximum Tolerated Dose
大体时间:5 weeks
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The maximum-tolerated dose (MTD) will be defined as the maximum dose level at which no more than one out of three subjects experience a dose-limiting toxicity (DLT) within the first 3 week of the first cycle of multiple dosing
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5 weeks
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次要结果测量
结果测量 |
大体时间 |
|---|---|
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SHR6390 的药代动力学参数评价:Cmax
大体时间:6周
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6周
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SHR6390 药代动力学参数评价:Tmax
大体时间:6周
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6周
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SHR6390药代动力学参数评价:t1/2
大体时间:6周
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6周
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SHR6390的药代动力学参数评价:AUC
大体时间:6周
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6周
|
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Number of patients experience adverse events
大体时间:up to 12 months
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up to 12 months
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Objective Response Rate
大体时间:every 8 weeks, up to 12 months
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every 8 weeks, up to 12 months
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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。
调查人员
- 首席研究员:Binhe Xu, M.D、Cancer Hosptial, Chinese Academy of Medical Sciences
出版物和有用的链接
负责输入研究信息的人员自愿提供这些出版物。这些可能与研究有关。
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)
2016年3月3日
初级完成 (实际的)
2019年6月28日
研究完成 (实际的)
2019年6月28日
研究注册日期
首次提交
2016年2月12日
首先提交符合 QC 标准的
2016年2月16日
首次发布 (估计)
2016年2月17日
研究记录更新
最后更新发布 (实际的)
2022年7月11日
上次提交的符合 QC 标准的更新
2022年7月7日
最后验证
2022年7月1日
更多信息
与本研究相关的术语
计划个人参与者数据 (IPD)
计划共享个人参与者数据 (IPD)?
未定
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.