NL-OMON44029已完成3 期
A randomized, double-blind, placebo-controlled, phase III multicenter study of subcutaneous secukinumab (150 mg) with and without a subcutaneous loading regimen to assess efficacy, safety, and tolerability up to 2 years in patients with active ankylosing spondylitis - MEASURE 4
试验速览
- 阶段
- 3 期
- 状态
- 已完成
- 发起方
- ovartis
- 入组人数
- 15
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 64（—）
入选标准
- •- Moderate to severe AS
- •- Prior radiographic evidence according to the Modified NY Criteria (1984)
- •- Inadequate response to NSAIDs;See protocol for other inclusion criteria.
排除标准
- •- Pregnancy or lactation
- •- On-going infectious or malignant process on a chest X-ray or MRI
- •- Previous exposure to IL-17 or IL-17R targeting therapies
- •- Previous exposure to any biological immunomodulating agent excluding TNF antagonists
- •- Previous cell depleting therapy;See protocol for other exclusion criteria.
研究者
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