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临床试验/JPRN-UMIN000007950
JPRN-UMIN000007950已完成2 期

Efficacy of ibritumomab tiuxetan (Zevalin) following remission induction therapy for relapse of follicular lymphoma - Ibritumomab tiuxetan (Zevalin) for relapse of follicular lymphoma

The University of Tokyo Hospital0 个研究点目标入组 25 人开始时间: 2012年5月15日最近更新:
适应症

试验速览

阶段
2 期
状态
已完成
入组人数
25

研究概览

简要总结

Entry completed

研究设计

研究类型
Observational

入排标准

年龄范围
20years-old 至 75years-old(—)
性别
All

入选标准

  • 未提供

排除标准

  • 1) Patients with uncontrollable infection. 2) Intolerable allergy for rituximab or drugs derived from murine proteins. 3) Previous history of allogeneic stem cell transplant. 4) Pregnant (or possibly pregnant) patient 5) Patients receiving anti-coagulants or anti-thrombotic agents. 6) Patients with hemorrhagic symptoms. 7) Patients receiving external radiation for more than 25% of total bone marrow. 8) Patients planning to undergo rituximab maintenance therapy.

研究者

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