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临床试验/JPRN-jRCT2080220936
JPRN-jRCT2080220936未知1 期

Phase 1 Study of CS-7017 - Evaluation of Safety and Pharmacokinetics of CS-7017 in Japanese Patients With Solid Cancer

DAIICHISANKYO Co.,Ltd.0 个研究点目标入组 12 人开始时间: 2009年12月11日最近更新:

试验速览

阶段
1 期
发起方
入组人数
12

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
>= 20age old 至 <= 75age old(—)
性别
All

入选标准

  • Histologically or cytologically diagnosed metastatic solid cancers which are not curable with, or not eligible for standard treatment(s)
  • -ECOG performance status: 0-1

排除标准

  • -History of any of the following events within 6 months prior to start of study treatment myocardial infraction, severe/unstable angina pectoris, coronary/peripheral artery bypass graft, congestive heart failure, cerebrovascular accident or cerebral infraction, pulmonary embolism, deep vein thrombosis, or other clinically significant thromboembolic event, clinically significant pulmonary disease (eg severe COPD or asthma)
  • -Patient with a clinically active brain metastasis, or who need drugs to control adverse event like edema and pleural effusion
  • -Inflammatory bowel disease, or partial bowel obstruction
  • -Patients with any severe or uncontrolled intercurent diseases

研究者

发起方
DAIICHISANKYO Co.,Ltd.

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