跳至主要内容
临床试验/jRCT2051200105
jRCT2051200105招募中不适用

Phase I / IIa, single-institution, open-label study to explore the safety and efficacy of R-OKY-034F long-term administration in patients with refractory / intolerable and surgically unresectable pancreatic cancer with standard chemotherapy

J-Pharma Co., Ltd.0 个研究点目标入组 30 人开始时间: 2019年9月17日最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
入组人数
30
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
分配方式
Single Arm Study
干预模型
Single Assignment
主要目的
Treatment Purpose
盲法
Open(masking Not Used)

入排标准

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

入选标准

  • Patients who are 20 years old or above at the time of informed consent
  • Patients with the ECOG performance status of 0 to 2 at the time of informed consent
  • Patients with a life expectancy of at least 90 days from the day of enrollment
  • Patients with a measurable lesion defined by the criteria of the RECIST version 1.1 according to the imaging during screening period
  • Patients judged by the (sub)investigator for whom the treatment may be continued R-OKY-034F-101 study

排除标准

  • Patients with active duplicate cancer
  • Patients with QTcE of over 500 msec
  • Patients weighing less than 40 kg at the time of informed consent
  • Patients who are considered inappropriate as a subject of this study by the (sub)investigator

结局指标

主要结局

-

Adverse Event and Side Effect

次要结局

  • Objective response rate
  • Disease control rate

研究者

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