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临床试验/EUCTR2019-001197-28-NL
EUCTR2019-001197-28-NL进行中(未招募)1 期

Can 89Zr-atezolizumab PET scan identify patients with metastatic invasive lobular breast cancer who will respond to chemotherapy-immune checkpoint inhibition? - ImaGelato

niversity Medical Center Groningen0 个研究点目标入组 10 人开始时间: 2019年4月11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
10

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
Female

入选标准

  • 1. A patient must meet the inclusion criteria of the GELATO trial (see in attachment the protocol)
  • 2. Able to give written informed consent and to comply with the ImaGelato protocol
  • 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 5
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range 5

排除标准

  • 1. Contra-indication for 89Zr-atezolizumab PET scan
  • 2. Any approved anti-cancer therapy, including chemotherapy or hormonal therapy within =14 days prior to the first 89Zr-atezolizumab injection. Treatment with any other investigational agent or participation in another clinical trial with therapeutic intent within 28 days prior to the first 89Zr-atezolizumab injection.

研究者

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