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临床试验/JPRN-UMIN000000501
JPRN-UMIN000000501已完成2 期

Phase II Study of Docetaxel and TS-1 Combination Therapy for Outpatients with Relapsed or Refractory Non-small Cell Lung cancer - Phase II Study of Docetaxel and TS-1 Combination Therapy for Relapsed or Refractory Non-small Cell Lung Cancer

Outpatient Oncology Unit Kyoto University Hospital0 个研究点目标入组 40 人开始时间: 2006年10月12日最近更新:
适应症

试验速览

阶段
2 期
状态
已完成
发起方
入组人数
40

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) Active ineterstitial pneumonitis 2) History of using TS-1 or docetaxel 3) Active infectious disease 4) Active hepatitis or hepatocirrhosis 5) Active concomitant malignancy 6) Uncontrollable diabetes 7) Serious cardiac disease 8) Psycologic illness 9) Other severe complications 10) Pleural or pericardial effusion, or ascites requiring treatment 11) Pregnant or lactation women, or women with known or suspected pregnancy and men who want let to pregnancy 12) Regular use of warfarin 13) Regular use of fenitoin or frucitocin 14) High fever 15) Clinical symptom of brain metastases 16) Serious nephropathy and/or edema 17) Regular use of steroid 18) Medical history of serious allergy reactions to any drug 19) Inappropriate patients for this study judged by the physicians.

研究者

发起方
Outpatient Oncology Unit Kyoto University Hospital

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