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临床试验/JPRN-UMIN000019828
JPRN-UMIN000019828已完成1 期

A phase I study of irinotecan, bevacizumab and biweekly TAS-102 in Japanese patients with metastatic colorectal cancer refractory to fluoropyrimidine and oxaliplatin - A phase I study of irinotecan, bevacizumab and biweekly TAS-102 in Japanese patients with metastatic colorectal cancer refractory to fluoropyrimidine and oxaliplatin (MODURATE study) MODURATE study

Pharma Valley Center0 个研究点目标入组 21 人开始时间: 2015年12月15日最近更新:
适应症

试验速览

阶段
1 期
状态
已完成
发起方
入组人数
21

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
20years-old 至 75years-old(—)
性别
All

入选标准

  • 未提供

排除标准

  • 1) Serious illness such as brain metastasis, systemic infection or gastrointestinal bleeding. 2) Medical treatment such as major surgery within 4 weeks, systemic chemotherapy within 2 weeks. 3) Adverse events due to prior chemotherapy 4) Administration of blood transfusion or G-CSF within 2 weeks 5) Severe pulmonaly disorder 6) Thromboembolism (grade3 or higher) within 6 months 7) Inappropriate for the study in the opinion of the investigator

研究者

发起方
Pharma Valley Center

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