NCT06154902进行中（未招募）不适用
ABE-DESCART Study: Characterization and Outcomes of Patients With Relapsed and Refractory Multiple Myeloma Eligible for Treatment or Treated With Abecma© (Idecabtagene Vicleucel) in Real World Setting in France. A Database Analysis Based on the DESCAR-T Registry
Bristol-Myers Squibb1 个研究点 分布在 1 个国家目标入组 350 人开始时间: 2022年7月29日最近更新:
适应症
干预措施
相关药物
试验速览
- 阶段
- 不适用
- 状态
- 进行中（未招募）
- 发起方
- 入组人数
- 350
- 试验地点
- 1
- 主要终点
- Overall survival
研究概览
简要总结
The purpose of this study is to describe demographic and disease characteristics, treatment patterns, and clinical outcomes in the real-world setting among participants in France with relapsed/refractory multiple myeloma (RRMM) who are eligible for treatment with, or have been treated with, idecabtagene vicleucel. This study will use both prospective and retrospective data from the DESCAR-T registry database.
研究设计
- 研究类型
- Observational
- 观察模型
- Cohort
- 时间视角
- Other
入排标准
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Patients with RRMM registered in the DESCAR-T registry and eligible for treatment or treated with idecabtagene vicleucel
排除标准
- •Not registered with the social security in France
研究组 & 干预措施
Treated with idecabtagene vicleucel
干预措施: Idecabtagene vicleucel (Drug)
Eligible for idecabtagene vicleucel
Eligible for idecabtagene vicleucel treatment but not treated
干预措施: Not treated (Other)
结局指标
主要结局
Overall survival
时间窗: 15 years
次要结局
未报告次要终点
研究者
研究点 (1)
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