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临床试验/EUCTR2021-000987-31-FR
EUCTR2021-000987-31-FR进行中(未招募)1 期

Immunomonitoring and multiple myeloma: impact of lenalidomide on immune checkpoint expression - IMMUNO-MYELO

CHU Rennes0 个研究点目标入组 22 人开始时间: 2021年3月15日最近更新:
适应症
相关药物

试验速览

阶段
1 期
状态
进行中(未招募)
发起方
CHU Rennes
入组人数
22

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

性别
All

入选标准

  • - Patient with newly diagnosed multiple myeloma;
  • - Patient not eligible for intensive treatment;
  • - Patient for whom first-line treatment with Lenalidomide-Dexamethasone will be initiated;
  • - Patient accepting the performance of an additional myelogram at the end of the 1st treatment cycle.
  • - Patient aged 18 years or older;
  • - Patient who has given free, informed and written consent;
  • - Patient affiliated to a social security scheme
  • - For women of childbearing age, use of effective contraception
  • 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 2
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range 20

排除标准

  • - Patient with relapsed multiple myeloma;
  • - Patient eligible for intensive treatment;
  • - Patient for whom chemotherapy involves treatment other than Lenalidomide-Dexamethasone;
  • - Patient with a contraindication to lenalidomide treatment
  • - Pregnant or breastfeeding woman;
  • - Person subject to legal protection (safeguard of justice, curatorship, guardianship) or person deprived of liberty.

研究者

发起方
CHU Rennes

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