跳至主要内容
临床试验/NL-OMON54892
NL-OMON54892尚未招募不适用

PRospective tumor sampling in oncology patients with solid tumors treated with Immune Modulating Agents - PRIMA

Erasmus MC, Universitair Medisch Centrum Rotterdam0 个研究点目标入组 350 人开始时间: 待定最近更新:

试验速览

阶段
不适用
状态
尚未招募
入组人数
350

研究概览

简要总结

暂无简介。

研究设计

研究类型
Observational

入排标准

年龄范围
18 至 99(—)

入选标准

  • Histological or cytological proven solid tumor
  • Age >=18 years
  • Written informed consent
  • Performance score: WHO 0-2 at the time of study entry
  • Planned treatment with (intravenous) immune modulating agents for any type of
  • cancer according to standard of care.

排除标准

  • Unable to draw blood for study purposes (e.g. severe anemia Hb <5,5 mmol/L)
  • Unable to safely obtain tumor biopsies
  • Known human immunodeficiency virus (HIV), chronic hepatitis B or C infection

研究者

相似试验