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临床试验/NCT02951091
NCT02951091已完成不适用

The Master Protocol for Biomarker-Integrated Umbrella Trial in Advanced Gastric Cancer

Yonsei University2 个研究点 分布在 2 个国家目标入组 400 人开始时间: 2016年1月1日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
400
试验地点
2
主要终点
progression free survival

研究概览

简要总结

In-depth understanding of molecular characteristics of gastric cancer enabled us to realize personalized medicine with targeted agents in gastric cancer treatment.

The investigators initiated open-label, randomized, controlled phase II, multi-arm trial comparing targeted therapy based on tumor molecular profiling with standard paclitaxel therapy as second line treatment.

详细描述

In-depth understanding of molecular characteristics of gastric cancer enabled us to realize personalized medicine with targeted agents in gastric cancer treatment.The investigators initiated open-label, randomized, controlled phase II, multi-arm trial comparing targeted therapy based on tumor molecular profiling with standard paclitaxel therapy as second line treatment.

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Parallel
主要目的
Diagnostic
盲法
None

入排标准

年龄范围
19 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Histologically or cytologically confirmed locally advanced or metastatic gastric cancer and gastroesophageal junction cancer
  • Eastern Cooperative Oncology Group performance status of 0 to 1
  • Male or female; ≥ 19 years of age
  • On or progression after 1st line palliative chemotherapy
  • Subjects with evaluable lesion (using RECIST 1.1 criteria)
  • Subjects who meet the following criteria:
  • Absolute neutrophil count ≥ 1000 /µL
  • Platelet count ≥ 75,000/ µL
  • Serum creatinine < 1.5 x upper limit of normal or Creatinine clearance ≥60 mL/min
  • aspartate aminotransferase and alanine transaminase 3 x upper limit of normal

排除标准

  • Evidence of any other significant clinical disorder or laboratory finding that makes it undesirable for the patient to participate in the study

结局指标

主要结局

progression free survival

时间窗: 6 weeks

progression free survival

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Sun Young Rha

professor

Yonsei University

研究点 (2)

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