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临床试验/JPRN-UMIN000010442
JPRN-UMIN000010442已完成1 期

Phase I study of FOLFOXIRI+Bev for unresectabl colorecatal cancer - Phase I study of FOLFOXIRI+Bev for unresectabl colorecatal cancer

Aichi Cancer Center Hospital0 个研究点目标入组 20 人开始时间: 2013年4月8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
20

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

  • Symptomatic brain metastasis Sever wattery diarrhea Paralytic or mechanical bowel obstruction Confirmed or suspected infection Severe pulmonary disease (interstitial pneumonia, pulmonary fobrosis, severe emphysematous) Severe comorbidity (uncontrolable diabetes, heart failure with NYHA 3 or 4, renal failure, liver failure) Pregnant or possibly pregnant, and nursing women Sever neurologic disease Receiving atazanavir sulfate Past history of monoclonal antibody allergy Past history of 5-FU/LV allergy Past history of FOLFOX allergy Complication of cerebrovascular disease or symptoms within 1 year Any surgical treatments including skin-open biopsy, trauma surgery and other more intensive surgery within 4 weeks or aspiration biopsy within one week Administering antithrombotic drug within 10 days Need to administrate or having anti-platelets therapy (including Methotrexate aspirin and NSAIDS) Evidence of bleeding diathesis or coagulopathy Active gastrointestinal ulcer Current or previous (within the last 1 year) history of GI perforation Non healing fracture Clinically significant (i.e. active) cardiovascular disease, or past or current history (within the last 1 year) of myocardial infarction Other conditions not suitable for this study

研究者

发起方
Aichi Cancer Center Hospital

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