EUCTR2012-002751-42-IT进行中（未招募）不适用
A randomized, double-blind, placebo-controlled, phase 3 study of brentuximab vedotin and CHP (A+CHP) versus CHOP in the frontline treatment of patients with CD30-positive mature T-cell lymphomas
Seattle Genetics, Inc.0 个研究点目标入组 300 人开始时间: 2013年2月26日最近更新:
适应症
相关药物
试验速览
- 阶段
- 不适用
- 状态
- 进行中（未招募）
- 发起方
- 入组人数
- 300
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
- •- ECOG performance less than or equal to 2
- •- Fluorodeoxyglucose (FDG)-avid disease by PET and measurable disease of at least 1.5 cm by CT
- •- Patients with newly diagnosed, CD-30-positive mature T-cell lymphomas
- •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 180
- •F.1.3 Elderly (>=65 years) yes
- •F.1.3.1 Number of subjects for this age range 120
排除标准
- •- Cerebral/meningeal disease related to the underlying malignancy
- •- Current diagnosis of primary cutaneous CD30-positive T-cell lymphoproliferative disorders and lymphomas or mycosis funoides
- •- History of another primary invasive malignancy that has not been in remission for at least 3 years
- •- History of progressive multifocal leukoencephalopathy (PML)
研究者
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