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临床试验/JPRN-UMIN000009993
JPRN-UMIN000009993已完成1 期

Phase I study on the feasibility of Nedaplatin plus S-1 combination therapy for squamous cell lung cancer. - Nedaplatin plus S-1 combination therapy for squamous cell lung cancer

Fukuoka University Hospital0 个研究点目标入组 18 人开始时间: 2013年2月18日最近更新:

试验速览

阶段
1 期
状态
已完成
入组人数
18

研究概览

简要总结

Because of shortage of case accumulation, the study was terminated.

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. Patient who have severe infection 2. Pregnant or lactating women. 3. Multiple cancer 4. A known history of allergy 5. A known history of GI bleeding 6. Patient who have interstitial pneumonia 7. Patient who have severe diabetes mellitus, liver cirrhosis, renal dysfunction, angina pectoris, arrhythmia, or myocardiac infarction before 3 months 8. Patient who have therapeutic need of pleural effusion, pericardiac effusion, or SVC syndrome 9. Patient who have obscure symptoms of brain metastasis. 10. Patient who have obscure symptoms of peripheral nerve dysfunction 11. Patient who take flucytosin.of brain 12. Patient who have severe 13.patient who is judged as an inappropriate case by the doctor in charge

研究者

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