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临床试验/NL-OMON30091
NL-OMON30091尚未招募3 期

A Double Blind, Randomized, Placebo Controlled, Multi-Center Trial of Anti-TNF alfa Chimeric Monoclonal Antibody (Infliximab, Remicade) and Azathioprine in Patients Suffering from Systemic Lupus Erythematosus (SLE) with WHO Class V Glomerulonephritis. - Trial V

Medical University of Vienna AKH, Department of Rheumatology, Internal Medicine III, Josef Smolen, MD0 个研究点目标入组 30 人开始时间: 待定最近更新:
适应症

试验速览

阶段
3 期
状态
尚未招募
发起方
入组人数
30

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
18 至 99(—)

入选标准

  • -SLE with biopsy-proven membranous glomerulonephritis (WHO class V)
  • -Proteinuria >3g/day despite adequate therapy with ACE inhibitors
  • -Individuals (>18 years) who have the capacity to understand and sign an informed consent
  • -No evidence of current active TB or old inactive TB

排除标准

  • -Active WHO class IV SLE nephritis
  • -Treatment with azathioprine / cyclophosphamide within the previous 12 months, or with cyclosporine within the previous 6 weeks
  • -Active cerebral SLE
  • -Active infection, malignancy

研究者

发起方
Medical University of Vienna AKH, Department of Rheumatology, Internal Medicine III, Josef Smolen, MD

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A Double Blind, Randomized, Placebo Controlled, Multi-Center Trial of Anti-TNFafa Chimeric Monoclonal Antibody (Infliximab, Remicade®) and Azathioprine in Patients Suffering from Systemic Lupus Erythematosus (SLE) with WHO Class V GlomerulonephritisSystemic Lupus Erythematosus (SLE) with WHO Class V Glomerulonephritis
EUCTR2005-004067-30-ATDepartment of Rheumatology, Internal Medicine III, Medical University of Vienna44