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Study of Metatinib Tromethamine Tablet

2017年1月20日 更新者:Jiangsu Simcere Pharmaceutical Co., Ltd.

A Phase Ib Clinical Study of the Tolerance, Safety and Preliminary Efficacy Observation of Single-/Multiple- Doses of Metatinib Tromethamine Tablets in Patients With Advanced or Metastatic Solid Tumor

This is an open-label, multicenter study designed to assess the safety, tolerability, preliminary efficacy and pharmacokinetics of Metatinib Tromethamine tablet in patients with advanced or metastatic gastric cancer, liver cancer, colorectal cancer,or con squamous NSCLC. Patients receive Metatinib orally 200mg once daily (QD) or 100mg twice daily (BID) until disease progression or unacceptable toxicity occurred. The study will determine whether MET gene mutation, amplification, as well as MET protein overexpression in tumor tissue correlate with treatment efficacy and clinical outcome. The potential PD biomarker for Metatinib will also be explored.

研究概览

研究类型

介入性

注册 (预期的)

24

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

    • Jilin
      • Changchun、Jilin、中国、130021
        • 招聘中
        • The First Bethune Hospital of Jilin University
        • 接触:
          • Yanhua Ding, MD
    • Sichuan
      • Chengdu、Sichuan、中国、610041
        • 招聘中
        • West China Hospital, Sichuan University
        • 接触:
          • Feng Bi, MD
    • Zhejiang
      • Hangzhou、Zhejiang、中国、310003
        • 招聘中
        • The First Affiliated Hospital, Zhejiang University

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 75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:

  • Patients with advanced or metastatic gastric cancer or colorectal cancer who progress after second-line therapy or the above treatment protocol, or patients with advanced or metastatic hepatocellular carcinoma who progress after first-line chemotherapy, interventional therapy or targeted therapy shall be verified by histology or cytology; or patients with advanced or metastatic non-squamous non-small cell lung cancer who cannot be operated or fail to first-line therapy shall be verified by histology or cytology;
  • MET gene amplification or protein overexpression(IHC ≥2+),or exon-14 skipping;
  • At least one measurable lesion (RECIST 1.1 );
  • At least 4 weeks from the last chemotherapy, radiotherapy or anti-tumor biological products treatment; at least 8 weeks from the last anti-tumor antibody products treatment; at least 6 weeks from the last dose of nitrosourea, mitomycin C or doxorubicin;
  • At least 4 weeks from major surgery or trauma, and the wound should fully heal; at least 1 week from minor surgery or trauma (i.e. tissue biopsy or fine needle aspiration);
  • Toxicity from previous treatment has to restore to ≤ grade 1, baseline or irreversible (NCI CTC4.0);
  • ECOG performance status 0-1;
  • Life expectancy ≥3 months;
  • Adequate hematologic function: ANC≥1.5×10^9 /L, HB≥90g/L(blood transfusion allowed), PLT≥100×10^9/L;
  • Adequate hepatic function: ALT≤3×ULN, AST≤3×ULN, TBIL≤2×ULN(patients with liver metastases or liver cancer ALT≤5×ULN, AST≤5×ULN, TBIL≤2×ULN), Child-Pugh score≤7;
  • Adequate renal function: uric acid<500μmol/L, creatinine<1.7mg/dL, proteinuria≤2+or≤2g/24h , GFR≥60 ml/min/1.73m^2;
  • PT-INR/APTT≤1.5×ULN, Serum sodium, potassium, calcium, magnesium levels ≤1×ULN(NCI-CTC 4.0);
  • Patients signed written informed consent;
  • Willingness and capability to comply with protocol requirement and well communicate with investigators.

Exclusion Criteria:

  • Severe, uncontrolled medical disorders or active infection, including but not limited to HIV antibody positive, active tuberculosis, HBV DNA copies>10^3/ml;
  • Subjects have known or suspected brain metastases;
  • Patients must receive other chemotherapy, targeted therapy, hormone therapy, immunotherapy, radiotherapy (except for palliative local radiation) or traditional Chinese medicine for treatment of cancer during the study;
  • Previously received other VEGF/VEGFR small-molecule inhibitors or antibodies therapy, including but not limited to Bevacizumab, Ramucirumab, Aflibercept;
  • Previously received other HGF/c-Met small-molecule inhibitors or antibodies therapy, including but not limited to Crizotinib, Cabozantinib, Volitinib, Capmatinib (INC280), BPI-9016M;
  • Imaging showed involvement of major blood vessels or nerves by tumor;
  • Uncontrolled hypertension (systolic blood pressure>150mmHg and/or diastolic blood pressure>100mmHg after treatment);
  • LVEF<50%;
  • Apparent heart disease, including congestive heart failure(NYHA III-IV), history of myocardial infarction, or uncontrolled angina within 6 months prior to enrollment;
  • Arrhythmias need to be treated, including atrial fibrillation, supraventricular tachycardia, ventricular tachycardia or ventricular fibrillation; ECG abnormalities confirmed, including QT interval prolongation (males>450msec, females>470 msec);
  • History of hemorrhagic or thrombotic events within 6 months before enrollment, i.e. cerebrovascular accidents(including TIA), pulmonary embolism, spontaneous hemorrhage of tumor;
  • Patients need surgery within 28 days, or is expected to require surgery within 28 days after the last dose;
  • Uncontrolled cavity effusion, such as large amount of pleural effusion and ascites;
  • Gastrointestinal illnesses(i.e., uncontrolled diarrhea or malabsorption) at screening or within 3 months that may affect drug absorption;
  • History or suspicious signs of gastrointestinal perforation;
  • Concomitant medications that may affect the drug metabolism (i.e. strong CYP3A4 inhibitors or inducer );
  • Pregnant or lactating women;
  • Subjects of childbearing refused to use medically acceptable methods of contraception until 3 months after the last dose;
  • Participate in other clinical trials within 4 weeks prior to enrollment;
  • The investigators consider the patients are not suitable for this trial

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:Metatinib Tromethamine
Patients receive Metatinib orally 200mg once daily (QD) or 100mg twice daily (BID) until disease progression or unacceptable toxicity occurred.

研究衡量的是什么?

主要结果指标

结果测量
大体时间
incidence of adverse events
大体时间:until 30 days after the last dose
until 30 days after the last dose

次要结果测量

结果测量
大体时间
Objective response rate
大体时间:every 6 weeks, up to 2 years
every 6 weeks, up to 2 years
Disease control rate
大体时间:every 6 weeks, up to 2 years
every 6 weeks, up to 2 years
Progression free survival
大体时间:every 6 weeks, up to 2 years
every 6 weeks, up to 2 years
Overall survival
大体时间:every 6 weeks, up to 2 years
every 6 weeks, up to 2 years
Cmax for Metatinib
大体时间:day 1,day 2,day 8,day15,day22
day 1,day 2,day 8,day15,day22
Cmin for Metatinib
大体时间:day 1,day 2,day 8,day15,day22
day 1,day 2,day 8,day15,day22
Tmax for Metatinib
大体时间:day 1,day 2,day 8,day15,day22
day 1,day 2,day 8,day15,day22
AUC for Metatinib
大体时间:day 1,day 2,day 8,day15,day22
day 1,day 2,day 8,day15,day22
T1/2 for Metatinib
大体时间:day 1,day 2,day 8,day15,day22
day 1,day 2,day 8,day15,day22
CL for Metatinib
大体时间:day 1,day 2,day 8,day15,day22
day 1,day 2,day 8,day15,day22

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:Feng Bi, MD、West China Hospital

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

2015年10月1日

初级完成 (预期的)

2017年10月1日

研究完成 (预期的)

2018年2月1日

研究注册日期

首次提交

2015年11月10日

首先提交符合 QC 标准的

2016年1月7日

首次发布 (估计)

2016年1月8日

研究记录更新

最后更新发布 (估计)

2017年1月23日

上次提交的符合 QC 标准的更新

2017年1月20日

最后验证

2017年1月1日

更多信息

与本研究相关的术语

其他研究编号

  • SIM-128-I-02

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.

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