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临床试验/JPRN-UMIN000009910
JPRN-UMIN000009910已完成2 期

A phaseII study of irinotecan with bevacizumab as third line treatment for patients with metastatic colorectal cancer after failure to irinotecan who have progressed on bevacizumab with oxaliplatin-based chemotherapy in second line. - A phaseII study of irinotecan with bevacizumab as third line treatment for patients with metastatic colorectal cancer after failure to irinotecan who have progressed on bevacizumab with oxaliplatin-based chemotherapy in second line.

Tsuchiura kyodo general hospital0 个研究点目标入组 25 人开始时间: 2013年1月30日最近更新:
适应症

试验速览

阶段
2 期
状态
已完成
入组人数
25

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) Need to drain malignant celomic fluid. (2)Radiological evidence of CNS metastases or brain cancer. (3) Multiple primary cancers within 5 years. (4) Complication of cerebrovascular disease or symptoms within 1 year. (5)Any surgical treatments including skin-open biopsy, trauma surgery and other more intensive surgery within 4 weeks or aspiration biopsy within one week. (6) The patient who is planning the surgical treatment during trial. (7)Administering antithrombotic drug within 10 days. (8)Need to administrate or having anti-platelets therapy (including Methotrexate aspirin and NSAIDS). (9) Evidence of bleeding diathesis or coagulopathy. (10)Active gastrointestinal ulcer (11)Current or previous (within the last 1 year) history of GI perforation. (12)Non healing fracture (13)Renal failure to be treated,3+ or higher proteinuria within 2 weeks prior to entry. (14)Uncontrolled Hypertension (15)Clinically significant (i.e. active) cardiovascular disease or past or current history (within the last 1 year) of myocardial infarction. (16)History of the serious hypersensitivity for irinotecan or bevacizumab. (17)Uncontrolled diarrhea (18)Evidence of interstinal lung disease, or pulmonary fibrosis. (19)History of organ transplantation. (20)Uncontrolled infection (21)Pregnant or lactating women or women of childbearing potential. (22) Men without the intention of preventing conception. (23) Other conditions not suitable for this study.

研究者

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