NL-OMON44667已完成3 期
An extension study to evaluate the sustainability of clinical benefits, safety and tolerability of secukinumab in patients with active Ankylosing Spondylitis (CAIN457F2305E1) - CAIN457F2305E1
适应症
试验速览
- 阶段
- 3 期
- 状态
- 已完成
- 发起方
- ovartis
- 入组人数
- 9
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
- •Subjects must have completed the core study
- •Subjects who are deemed by the investigator to benefit from continued secukinumab therapy
排除标准
- •Any subject taking other concomitant biologic immunomodulating agent(s) except secukinumab during the core study
- •Pregnancy, lactation.
- •Women of childbearing potential who do not use adequate contraception.
研究者
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