NL-OMON52719招募中4 期
Comparison of subcutaneous and intravenous retreatment with ultra-low dose rituximab in rheumatoid arthritis: a randomised open-label non-inferiority trial - RTX-SC
适应症
试验速览
- 阶段
- 4 期
- 状态
- 招募中
- 入组人数
- 36
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
- •- Rheumatoid arthritis: either 2010 EULAR/ACR RA17 and/or 1987 ACR RA18
- •criteria and/or clinical diagnosis of the treating rheumatologist;
- •- Patients using rituximab in ultra-low dose: either 200 mg or 500 mg as
- •previous dose, given every 6 months, with or without concomitant methotrexate;
- •- Having sufficient response to rituximab treatment, operationalized as a
- •DAS28-CRP < 2.9 3-6 months after the last infusion and/or judgment of low
- •disease activity by the treating rheumatologist;
- •- >=16 years old and mentally competent;
- •- Ability to read and communicate well in Dutch.
排除标准
- •- Previous non-response to ultra-low dose rituximab (DAS28-CRP > 2.9);
- •- Objection or contraindication to either of the treatment options.
研究者
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