EUCTR2015-003286-28-FR进行中（未招募）不适用
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
相关药物
试验速览
- 阶段
- 不适用
- 状态
- 进行中（未招募）
- 入组人数
- 120
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) and relapsed/refractory
- •Cutaneous T Cell Lymphoma (CTCL)
- •Mycosis Fungoides/Sezary Syndrome (MF/SS)
- •Expression of CD30
- •Subjects must be 18 years or older
- •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 60
- •F.1.3 Elderly (>=65 years) yes
- •F.1.3.1 Number of subjects for this age range 60
排除标准
- •Known central nervous system (CNS)
- •lymphomas; Active
- •cerebral/meningeal disease related
- •to the underlying malignancy
- •Active, known, or suspected autoimmune disease
研究者
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