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临床试验/NCT00556192
NCT00556192已完成2 期

Can Targeted Elimination of B-cell Depletion Therapy and/or Combination Therapy Restore Peripheral B Cell Abnormalities in Systemic Lupus Erythematosus(SLE)?

Chinese University of Hong Kong1 个研究点 分布在 1 个国家目标入组 20 人开始时间: 2006年6月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
2 期
状态
已完成
入组人数
20
试验地点
1
主要终点
-Estimated glomerular filtration rate(FRR) of >90 mil/minute.1.73m2 -Urinary protein:urinary creatinine ratio of <0.2 -Inactive urinary sediment

研究概览

简要总结

This prospective randomized control trial is undertaken to evaluate the safety and efficacy of anti-CD20 monoclonal antibody, rituximab, used as 1. monotherapy, 2. in combination with cyclophosphamide, in the treatment of proliferative lupus nephritis, as compared with standard immunosuppressive therapy with cyclophosphamide and azathioprine.

详细描述

Twenty patients will be randomized into 3 treatment arms to receive:

  • Rituximab of 1000 mg given 2 weeks apart. On day the of rituximab, and 'pulse' methylprednisolone 250mg IV be given followed by prednisolone 30mg/day from Day 2 to Day 5.
  • A treatment dose rituximab of 1000mg given 2 weeks apart and 'pulse' methylprednisolone 250mg IV be given followed by prednisolone 30mg/day from Day 2 to Day 5, and 'pulse' cyclophosphamide 500mg/m2 at baseline and day 14.
  • Sequential therapy with oral cyclophosphamide (50 to 100 mg/day) for 6 months followed by azathioprine (up to 2.5mg/kg/day) for maintenance up to 12 months. Oral prednisolone will be given at 0.5 mg/kg/day (up to 30 mg daily) for 4 weeks, tapered by 5 mg every 2 weeks thereafter until 5mg /day for the rest of the study period. All patients would be started on angiotensin converting enzyme inhibitors before commencement of the trial and to continue at the same dosage throughout the study period. Patients who are on antimalarial agents and statins at baseline will be allowed to continue.

Clinical examination and laboratory investigations will be performed at 0, 4, 8, 12, 24, 36 and 48 weeks from the time of treatment. At each visit, patients will be evaluated for clinical manifestation of SLE and side effects of therapy. Laboratory parameters measured included the complete blood cell count with differential and platelet counts, chemistries survey, urinalysis, and 24- hour urinary for protein excretion and creatinine clearance.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

入排标准

年龄范围
18 Years 至 70 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Age > 18 years
  • Active proliferative lupus nephrites
  • Biopsy confirmed active proliferative lupus nephritis within 3 months prior to enrollment
  • Proteinuria >= 2g/day
  • Active urinary sediments
  • Activity index of >= 6
  • Elevated anti-double-stranded(anti-dsDNA) level at baseline
  • Agreement to practice birth control
  • SLE according to the American College of Rheumatology Criteria
  • Informed consent was obtained

排除标准

  • Pre-existing renal failure
  • History of cancer
  • Human immunodeficiency virus infection
  • Active hepatitis B or C infection
  • Active tuberculosis
  • Diabetes mellitus
  • A ny other chronic disease
  • Unwillingness to comply with the protocol

研究组 & 干预措施

1

Active Comparator

Rituximab

干预措施: rituximab (Drug)

2

Active Comparator

Rituximab + Cyclophosphamide

干预措施: rituximab (Drug)

3

Active Comparator

Cyclophosphamide

干预措施: rituximab (Drug)

结局指标

主要结局

-Estimated glomerular filtration rate(FRR) of >90 mil/minute.1.73m2 -Urinary protein:urinary creatinine ratio of <0.2 -Inactive urinary sediment

时间窗: wk48

次要结局

  • -The estimated GFR,urinary protein values and urinary sediment -Changes in disease activity score(SLEDAI) -Other clinical features -Duration of B-cell depletion(baseline,wk0,wk4,wk8,wk12,wk24,wk36,wk48)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Lai-Shan Tam

Professor

Chinese University of Hong Kong

研究点 (1)

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