跳至主要内容
临床试验/JPRN-jRCT2080221196
JPRN-jRCT2080221196未知1 期

A phase I study of NK105 administrated weekly in patients with advanced solid malignancies.

ippon Kayaku Co., Ltd.0 个研究点目标入组 25 人开始时间: 2010年8月11日最近更新:

试验速览

阶段
1 期
发起方
入组人数
25

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 <= 74age old(—)
性别
All

入选标准

  • Histologically or cytologically confirmed malignant solid tumour.
  • Refractory to standard therapy or for which no suitable effective standard therapy exists.

排除标准

  • Treated with taxanes within 6 months

研究者

发起方
ippon Kayaku Co., Ltd.

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