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临床试验/JPRN-jRCT2080221457
JPRN-jRCT2080221457未知1 期

A Phase 1 Study of LY2523355 in Patients with Solid Cancer

Kyowa Hakko Kirin Co., Ltd.0 个研究点开始时间: 2011年5月17日最近更新:

试验速览

阶段
1 期
发起方

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 ot applicable(—)
性别
All

入选标准

  • Histological and/or cytological evidence of solid tumors
  • - A diagnosis of advanced and/or metastatic solid tumors
  • - Patients who are refractory to standard therapy or for which no proven effective therapy exists
  • - Written informed consent
  • - Appropriate bone marrow, hepatic and renal functions
  • - ECOG PS =< 1

排除标准

  • - Have serious preexisting complication
  • - Have active infection which requires intravenous antibiotics
  • - Have symptomatic central nervous system metastases
  • - Have current acute or chronic leukemia
  • - Have had an autologous or allogenic hematopoietic stem cell transplantation
  • - Have active multiple cancers

研究者

发起方
Kyowa Hakko Kirin Co., Ltd.

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