跳至主要内容
临床试验/JPRN-UMIN000003332
JPRN-UMIN000003332已完成未知

Phase I/II study of nedaplatin, a cisplatin analogue, and S-1 in patients with advanced squamous cell lung carcinoma. - Phase I/II study of nedaplatin, a cisplatin analogue, and S-1 in patients with advanced squamous cell lung carcinoma.

Keio University School of Medicine, division of Pulmonary Medicine0 个研究点目标入组 45 人开始时间: 2010年3月15日最近更新:

试验速览

阶段
未知
状态
已完成
发起方
入组人数
45

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 80years-old(—)
性别
All

入选标准

  • 未提供

排除标准

  • 1.History of grave drug allergic reaction 2.Patients under treatment with phenytoin or flucytosine. 3.Serious complications (e.g. intestinal paralysis, intestinal obstruction, interstitial pneumonia or fibroid lung detectable on chest X-ray films , poorly controlled diabetes, heart failure, renal failure, hepatic failure, or haemorrhagic peptic ulcer etc.). Serious medical complications 4. History of poorly controlled pleural effusion,pericardial effusion and ascites . 5.Symptomatic brain metastasis 6.Patients with uncontrolled water diarrhea or chronic constipation. 7.Active double cancer. Carcinoma in situ and lesions of intramucosal carcinoma will not be included in active double cancer and will be permitted for registration. 8.Pregnant females, possibly pregnant females, females wishing to become pregnant and nursing mothers. 9.Males that are currently attempting to produce a pregnancy. 10.Inadequate physical condition, as diagnosed by primary physician.

研究者

发起方
Keio University School of Medicine, division of Pulmonary Medicine

相似试验