NCT01095393已完成不适用
National Data Bank for Rheumatic Disease (NDB) Registry Study of Safety in Rheumatoid Arthritis (RA) Patients Treated With Certolizumab Pegol (CZP; Cimzia®) and Non-biologic Disease-modifying Antirheumatic Drug (DMARD) Therapies
适应症
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- UCB Pharma
- 入组人数
- 12,500
- 主要终点
- Number of participants with lymphoma
研究概览
简要总结
Observational registry to assess the longer-term risk of serious infections and malignancies reported with TNFα-blocker therapy, as well as the longer-term risk of cardiovascular and thromboembolic events in adult Rheumatoid Arthritis (RA) patients treated with Cimzia® as compared to non-biologic DMARD-treated controls.
研究设计
- 研究类型
- Observational
- 观察模型
- Cohort
- 时间视角
- Prospective
入排标准
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •RA and started treatment with certolizumab pegol (Cimzia®; CZP) or non-biologic DMARD within the last 6 months
排除标准
- 未提供
结局指标
主要结局
Number of participants with lymphoma
时间窗: 6 years
Number of participants with lymphoma during the observational period (up to 6 years)
次要结局
- Number of participants with serious infections(6 years)
- Number of participants with non-lymphoma malignancies(6 years)
- Number of participants with cardiovascular events(6 years)
- Number of participants with thromboembolic events(6 years)
研究者
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