跳至主要内容
临床试验/EUCTR2015-003286-28-IT
EUCTR2015-003286-28-IT进行中(未招募)1 期

A Phase I/ II Study to Evaluate the Safety and Preliminary Efficacy of Nivolumab in Combination with Brentuximab Vedotin in Subjects with Relapsed Refractory Non Hodgkin Lymphomas with CD30 Expression - CheckMate 436: CHECKpoint pathway and nivolumab clinical Trail Evaluation

BRISTOL-MYERS SQUIBB INTERNATIONAL CORPORATIO0 个研究点目标入组 170 人开始时间: 2021年6月17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)
入组人数
170

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

  • Relapsed/refractory diffuse large B cell lymphoma (DLBCL),
  • relapsed/refractory peripheral T cell lymphoma (PTCL) (all subtypes
  • excluding anaplastic large cell lymphoma), relapsed/refractory
  • Cutaneous T cell lymphoma (CTCL) mycosis fungoides/sezary syndrome
  • (MF/SS), relapsed/refractory primary mediastinal B lymphoma (PMBL),
  • and relapsed/refractory mediastinal gray zone lymphoma (MGZL)
  • Expression of CD30
  • Subjects must be 18 years or older (= 15 years for PMBL)
  • Are the trial subjects under 18? yes
  • 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 85
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range 80

排除标准

  • - Location of the NHL in the central nervous system (CNS)
  • - Positive test for autoimmune disease

研究者

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