跳至主要内容
临床试验/NCT02799199
NCT02799199已完成不适用

Fingolimod Real World Experience: the French Grand-Est Cohort

CHU de Reims0 个研究点目标入组 1,014 人开始时间: 2014年9月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
CHU de Reims
入组人数
1,014
主要终点
the course of the disease by magnetic resonance imaging (MRI)

研究概览

简要总结

Objectives: This study describes efficacy and safety of Fingolimod in patients treated for at least 6 months in the east of France from January 2011 to December 2014.

Background: The Grand-Est is a geographical region in France with a high prevalence of multiple sclerosis (more than 10000 patients registered in the European Database for Multiple Sclerosis (EDMUS) database). In this region and since January 2011, more than 1014 patients have been treated for at least 6 months with Fingolimod, the first oral therapy for patient with very active relapsing-remitting MS.

Methods: Features of patients followed up in the Grand-Est region and treated with fingolimod in the 6 university hospitals, general hospitals and private neurologists were reviewed in a retrospective study after identification of the clinical files reported in the EDMUS database.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Retrospective

入排标准

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

入选标准

  • Patients with MS treated with Gilenya because of the disease

排除标准

  • contraindications of Gilenya treatment or receiving Gilenya after the 31st of March 2014

结局指标

主要结局

the course of the disease by magnetic resonance imaging (MRI)

时间窗: assessed between January 2012 and September 2014, up to a total of 32 months

次要结局

未报告次要终点

研究者

发起方
CHU de Reims
申办方类型
Other
责任方
Sponsor

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