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临床试验/JPRN-UMIN000005077
JPRN-UMIN000005077已完成2 期

Phase II Study of Docetaxel+Bevacizumab with non-squamous non-small cell lung cancer for patients pretreated with chemotherapy - Phase II Study of Docetaxel+Bevacizumab with non-squamous non-small cell lung cancer for patients pretreated with chemotherapy

Tochigi Cancer Center0 个研究点目标入组 22 人开始时间: 2011年2月14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
22

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)Symptomatic Brain metastasis or expected bleeding. 2) history of active double cancer within 5 years. 3) Severe infection 4) History of hemoptysis with 2.5mL or more. 5) Continued bloody phlegm. 6) Receiving anticoagulant drug(including Aspirin over 325mg/day). 7) Perforation of the digestive tract or history of the perforation of the digestive tract within the past one year. 8) Severe comorbidity (heart failure Tendency to hemorrhages uncontrollable hypertension, uncontrollable diabetes, etc) 9) Arterial thromboembolism and Venous thromboembolism within the past one year. 10)Interstitial pneumonia or pulmonary fibrosis detectable on X ray. 11) Neuropathy or edema 12) History of hypersensitivity reaction to drugs formulated with polysorbate. 13) Planning of surgery or thoracic radiotherapy during the trial. 14) Major surgical procedure 15) With a history of drug sensitivity. 16) Pregnant or lactating women or those who declined contraception. 17) Any other medical condition that makes the patient unsuitable for inclusion in the study according to the opinion of the investigator.

研究者

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