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临床试验/EUCTR2017-003466-28-ES
EUCTR2017-003466-28-ES进行中(未招募)1 期

A Phase 2, multicenter, open-label study of DS-8201a in subjects with HER2-expressing advanced colorectal cancer

Daiichi Sankyo Inc.0 个研究点目标入组 78 人开始时间: 2018年3月7日最近更新:
适应症

试验速览

阶段
1 期
状态
进行中(未招募)
入组人数
78

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional clinical trial of medicinal product

入排标准

性别
All

入选标准

  • - Has pathologically documented unresectable, recurrent, or metastatic
  • colorectal adenocarcinoma (until sponsor's notification to the study
  • sites, subject must be a RAS/BRAF wild-type cancer)
  • - Has received at least 2 prior regimens of standard treatment
  • - Has measurable disease assessed by the investigator based on RECIST
  • version 1.1.
  • - Has an Eastern Cooperative Oncology Group Performance Status (ECOGPS) of 0 to 1
  • Are the trial subjects under 18? no
  • Number of subjects for this age range:
  • F.1.2 Adults (18-64 years) yes
  • F.1.2.1 Number of subjects for this age range 80
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range 10

排除标准

  • - Has a medical history of myocardial infarction within 6 months, symptomatic congestive heart failure
  • - Has a history of (non-infectious) ILD/pneumonitis that required steroids, has current ILD/pneumonitis, or where suspected ILD/pneumonitis cannot be ruled out by imaging at screening.
  • - Has spinal cord compression or clinically active central nervous system metastases, defined as untreated and symptomatic, or requiring therapy

研究者

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