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临床试验/JPRN-jRCT2080225077
JPRN-jRCT2080225077已完成1 期

A PHASE I STUDY OF RO7082859 IN PATIENTS WITH B-CELL NON-HODGKIN'S LYMPHOMA

Chugai Pharmaceutical Co., Ltd.0 个研究点目标入组 12 人开始时间: 2020年2月18日最近更新:
适应症

试验速览

阶段
1 期
状态
已完成
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
>= 20age old 至 ot applicable(—)
性别
All

入选标准

  • CD20 positive B cell NHL that is recurrent or refractory to standard therapy or for which no standard therapy exists.
  • - Pathologically confirmed B cell NHL.
  • - ECOG PS of 0 or 1.
  • - Life expectancy =>12 weeks from the date of enrollment.
  • - Major organ function meets all criteria.

排除标准

  • - Pregnant or lactating woman.
  • - Current or previous autoimmune disease.
  • - Positive test result for human immunodeficiency virus antibody, hepatitis B surface antigen, HBs antibody, hepatitis B core antibody, or hepatitis C virus antibody.
  • - Current or previous clinically significant liver disease.
  • - Current central nervous system lymphoma, metastases to the CNS, or meningeal metastases.
  • - History of previous therapy with allogenic hematopoietic stem cell transplantation or solid organ transplantation.
  • - History of severe allergic or anaphylactic reactions to monoclonal antibody therapy or fusion proteins.

研究者

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