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临床试验/JPRN-jRCT2080222962
JPRN-jRCT2080222962未知1 期

A Phase 1 Study of LY2606368 in Japanese Patients with Advanced Solid Tumors

Eli Lilly Japan K.K.0 个研究点开始时间: 2015年9月9日最近更新:
适应症

试验速览

阶段
1 期

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

  • Participant must be appropriate candidate for experimental therapy, as determined by investigator, after available standard therapies have failed
  • Participant must have diagnosis of cancer that is advanced or metastatic
  • Participant must have discontinued previous treatments for cancer and recovered from the acute effects of that therapy
  • If participant is of reproductive potential, must agree to use medically approved contraceptive precautions during the study and for three months following the last dose of study drug
  • If the participant is a female of childbearing potential, must have had a negative serum or urine pregnancy test within 7 days of the first dose of study drug and must not be breast feeding
  • Participant must not have symptomatic central nervous system malignancy or metastasis
  • Participant must not have current hematologic malignancy
  • Participant must not have an active symptomatic fungal, bacterial or viral infection, including human immunodeficiency virus (HIV) or Hepatitis A, B, or C
  • Participant must not have a serious cardiac condition

排除标准

  • 未提供

研究者

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