JPRN-jRCT2080222962未知1 期
A Phase 1 Study of LY2606368 in Japanese Patients with Advanced Solid Tumors
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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