NCT00234897已完成4 期
Humira Efficacy Response Optimization Study in Subjects With Active Rheumatoid Arthritis (HERO)
Abbott1 个研究点 分布在 1 个国家目标入组 1,938 人开始时间: 2004年8月1日最近更新:
适应症
干预措施
相关药物
试验速览
- 阶段
- 4 期
- 状态
- 已完成
- 发起方
- 入组人数
- 1,938
- 试验地点
- 1
- 主要终点
- Patient reported outcomes, clinical response indicators.
研究概览
简要总结
The purpose of the study is to assess the efficacy of adalimumab in subjects with rheumatoid arthritis focusing on subject-reported outcomes and early response to treatment
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
- Double
入排标准
- 年龄范围
- 18 Years 至 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Subject was age 18 or older and in good health (Investigator discretion) with a recent stable medical history.
- •Subject, based on assessment of investigator, meets the definition of active RA
排除标准
- •Subject considered by the investigator, for any reason, to be an unsuitable candidate for the study
- •Female subject who is pregnant or breast-feeding or considering becoming pregnant
研究组 & 干预措施
未命名试验
干预措施: adalimumab (Drug)
结局指标
主要结局
Patient reported outcomes, clinical response indicators.
次要结局
- Subject reported assessments of disease activity, physician reported assessments of disease activity, safety parameters, clinical response indicators.
研究者
研究点 (1)
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