跳至主要内容
临床试验/jRCT2080222238
jRCT2080222238未知2 期

Phase II trial of YHI-1003 monotherapy in patients with advanced or relapsed gynecologic cancer

Yakult Honsha Co., Ltd.0 个研究点目标入组 96 人开始时间: 待定
适应症

试验速览

阶段
2 期
入组人数
96
主要终点
-

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional
干预模型
Open-label, Multicenter Trial

入排标准

年龄范围
20age old over 至 No limit(—)
性别
Female

入选标准

  • •(1)Patients with a histologically-diagnosed ovarian , endometric or cervical cancer
  • •(2)Patients with a history of treatment with platinum-based chemotherary
  • •(3)Patients who have agreed with the investigation of biomarkers
  • •(4)Patients who can be treated with oral medications
  • •(5)Patients with at least one measurable disease

排除标准

  • •(1)Patients with a history of treatment with PI3K, AKT or mTOR inhibitor
  • •(2)Patients with uncontrolled intercurrent illness
  • •(3)Patients with brain metastases or suspected brain metastases

结局指标

主要结局

-

Disease Control Rate RECIST ver1.1

次要结局

未报告次要终点

研究者

相似试验