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临床试验/JPRN-jRCT2080224117
JPRN-jRCT2080224117已完成1 期

PHASE 1/2 STUDY OF TAS-120 IN PATIENTS WITH ADVANCED SOLID TUMORS HARBORING FGF/FGFR ABERRATIONS

Taiho Pharmaceutical Co., Ltd.0 个研究点目标入组 20 人开始时间: 2018年10月29日最近更新:

试验速览

阶段
1 期
状态
已完成
入组人数
20

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

  • 1. Provide written informed consent.
  • 2. Is >= 20 years.
  • 3. Has histologically or cytologically confirmed, locally advanced, metastatic cancer.
  • 4. Patient has measurable disease.
  • 5. ECOG performance status 0 or 1.
  • 6. Able to take medications orally.
  • 7. Adequate organ function.
  • 8. Have a negative pregnancy test.
  • 9. Willing and able to comply with scheduled visits and study procedures.

排除标准

  • 1. History and/or current evidence of non-tumor related alteration of calcium-phosphorus homeostasis.
  • 2. History and/or current evidence of clinically significant ectopic mineralization/calcification.
  • 3. History and/or current evidence of clinically significant retinal disorder confirmed by retinal examination.
  • 4. A serious illness or medical condition(s)

研究者

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