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临床试验/JPRN-jRCT2080220627
JPRN-jRCT2080220627未知2 期

Dose-Response Study of Ocrelizumab for Rheumatoid Arthritis.

Chugai Pharmaceutical Co., Ltd.0 个研究点开始时间: 2008年10月23日最近更新:
适应症

试验速览

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

  • Diagnosis of RA for >=6 months according to the revised 1987 ACR criteria for the classification of RA.
  • - Receiving methotrexate at a dose of 6 to 8 mg/week(oral) for >=12 weeks, with a stable dose for the last 4 weeks before treatment.
  • - Positive serum RF.

排除标准

  • - Rheumatic autoimmune disease other than RA, or Significant systemic involvement secondary to RA. Patients with secondary Sjogren's syndrome or secondary limited cutaneous vasculitis with RA are eligible.
  • - Functional Class IV as defined by the ACR Classification of Functional Status in RA.
  • - History of or current inflammatory joint disease other than RA or other systemic autoimmune disorder.
  • - Any surgical procedure within 12 weeks prior to or planned within 24 weeks after baseline.

研究者

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