EUCTR2020-003874-30-IT进行中（未招募）1 期
A 2-year follow-up study to assess cognition and health-related quality of life in participants with highly-active relapsing multiple sclerosis, having participated in the CLARIFY MS trial - CLARIFY MS Extension
相关药物
试验速览
- 阶段
- 1 期
- 状态
- 进行中（未招募）
- 发起方
- MERCK KGAA
- 入组人数
- 320
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional clinical trial of medicinal product
入排标准
- 性别
- All
入选标准
- •1. Participants having participated in the CLARIFY MS trial, who:
- •a. Have at least CLARIFY MS Baseline data on SDMT;
- •b. Received at least a single dose of cladribine tablets in the CLARIFY MS trial; and
- •c. Completed the Final Study Visit (M24) of the CLARIFY MS trial.
- •2. Capable of giving signed informed consent, which includes compliance
- •with the requirements and restrictions listed in the informed consent
- •form (ICF) and this protocol.
- •Are the trial subjects under 18? no
- •Number of subjects for this age range:
- •F.1.2 Adults (18-64 years) yes
- •F.1.2.1 Number of subjects for this age range 318
- •F.1.3 Elderly (>=65 years) yes
- •F.1.3.1 Number of subjects for this age range 2
排除标准
- •1. Participant is considered by the Investigator and Sponsor, for any reason, to be an unsuitable candidate for the study.
- •2. Participation in other studies/trials.
研究者
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