跳至主要内容
临床试验/NCT00664573
NCT00664573终止2 期

Assessment of Safety and Efficacy of BG9924 in Subjects With RA Who Have Participated in Study 104RA202.

Biogen9 个研究点 分布在 8 个国家目标入组 339 人开始时间: 2007年11月1日最近更新:
适应症

试验速览

阶段
2 期
状态
终止
发起方
Biogen
入组人数
339
试验地点
9
主要终点
To Observe The Long-Term treatment with BG9924 When Administered to Participants with RA who Previously Participated in a Biogen Idec Study

研究概览

简要总结

To observe the long-term treatment with BG9924 when administered to participants with RA who previously participated in a Biogen Idec Study.

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 (Participant, Investigator)

入排标准

年龄范围
18 Years 至 75 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Must be a participant from Study 104RA202 (NCT 00664716)
  • Stable dose of Methotrexate for the duration of the study

排除标准

  • Participants with a significant change in their medical history from their previous BG9924 study
  • Any clinically significant infectious illness or serious local infection
  • NOTE: Other protocol defined Inclusion/Exclusion criteria may apply.

结局指标

主要结局

To Observe The Long-Term treatment with BG9924 When Administered to Participants with RA who Previously Participated in a Biogen Idec Study

时间窗: Duration of this study is 18 months

次要结局

未报告次要终点

研究者

发起方
Biogen
申办方类型
Industry
责任方
Sponsor

研究点 (9)

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