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临床试验/JPRN-UMIN000003867
JPRN-UMIN000003867已完成1 期

Phase 1 study of fludarabine combined with rituximab followed by Zevalin for patients with relapsed or refractory indolent B cell lymphoma - Fludarabine combined with rituximab followed by Zevalin for patients with relapsed or refractory indolent B cell lymphoma

Tohoku Hematology Form0 个研究点目标入组 12 人开始时间: 2010年7月5日最近更新:
适应症

试验速览

阶段
1 期
状态
已完成
发起方
入组人数
12

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

年龄范围
20years-old 至 79years-old(—)
性别
All

入选标准

  • 未提供

排除标准

  • (a)History of hematopoietic stem cell transplantation (b)History of whole pelvic or whole abdomen radiation (c)Received G-CSF or erythropoietin or transfusion less than one week before registration (d)Taken an operation less than four weeks before registration (e)History of Zevalin therapy (f)History of the treatment of purin analogs (g)Have active systemic infections (h)Have a serious complication(cardiac dysfunction, hepatic failure, or renal failure) (i)Have a serious digestive organ symptom (j)Have a serious bleeding tendency (k) Positive for HBs antigen, HCV antibody, or HIV antibody. (l)Have an interstitial pneumonia or fibrosis (m)Active cancers (n)Have or history of autoimmune hemolytic anemia (o)Have aglucoma (p) Otherwise judged by investigator to be unsuitable

研究者

发起方
Tohoku Hematology Form

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