DRKS00034406招募中不适用
on-interventional, prospective, multicenter study to evaluate treatment satisfaction, treatment preference, quality of life, and tolerability under treatment with Briumvi® for relapsing forms of multiple sclerosis (RMS) with active disease in daily clinical practice - Briumvi® - Real World Experience Study (BRILL Study)
euraxpharm Pharmaceuticals, S.L.0 个研究点目标入组 600 人开始时间: 2024年6月11日最近更新:
适应症
试验速览
- 阶段
- 不适用
- 状态
- 招募中
- 发起方
- 入组人数
- 600
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Observational
入排标准
- 年龄范围
- 18 Years 至 one（—）
- 性别
- All
入选标准
- •Established clinical diagnosis of RMS with active disease.
- •- Having been prescribed treatment with Briumvi® according to label and treatment is already initiated, with enrollment occurring no more than 90 days after the first dose.
- •Patient with newly prescribed Briumvi® in accordance with the label and about to start treatment with Briumvi® at Visit 1.
- •- Ability to understand the purpose and risks of the study and willing to provide signed and dated study-specific ICF.
排除标准
- •Patient cannot be regularly followed up for organizational or geographic reasons.
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