跳至主要内容
临床试验/JPRN-UMIN000002761
JPRN-UMIN000002761招募中2 期

Phase II trial of irinotecan with biweekly cetuximab in unresectable advanced and/or metastatic colorectal cancer, evaluation of the safety and efficacy based on EGFR positive and KRAS wild type.(i-BEX trial) - Phase II trial of irinotecan with biweekly cetuximab in advanced and/or metastatic colorectal cancer.(i-BEX trial)

PO FMPC (Future Medicine Promoting Consortium)0 个研究点目标入组 45 人开始时间: 2009年11月16日最近更新:
适应症

试验速览

阶段
2 期
状态
招募中
发起方
入组人数
45

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 ot applicable(—)
性别
All

入选标准

  • 未提供

排除标准

  • 1)history of severe allergy 2)severe complications paralytic or mechanical bowel obstruction interstitial lung disease pulmonary fibrosis heart failure liver failure renal insufficiency 3)Patients who had received at least cetuximab contained chemotherapy 4)Patients who are impossible to receive irinotecan contained chemotherapy severe infectious disease watery diarrhea massive pleural effusion or ascites Jaundice Patients who is receiving Atazanavir Sulfate 5)Pregnant or lactating women or women of childbearing potential 6)Symptomatic brain metastasis 7)Patients with active double cancer 8)Patients who are considered unfit for enrollment in the study because of mental illness, etc. of clinical relevance 9)Patients with heart disease of clinical relevance 10)Inadequate physical condition, as diagnosed by primary physician

研究者

发起方
PO FMPC (Future Medicine Promoting Consortium)

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