Teriflunomide's Therapeutic Mechanisms of Action in Patients With Relapsing Remitting Multiple Sclerosis.
2017年9月14日 更新者:University of North Carolina, Chapel Hill
Characterization of Teriflunomide's Therapeutic Mechanisms of Action in Patients With Relapsing Remitting Multiple Sclerosis.
The purpose of this research is to characterize the effect of teriflunomide on the activation of B-cells, as well as its capacity to modify B-cell cytokine secretion.
The in-vitro identified effects of teriflunomide on the expression of B-cell activation markers, costimulatory and antigen presenting molecules, as well as on cytokine secretion, will then be confirmed in a cohort of Relapsing Remitting Multiple Sclerosis (RRMS) patients treated with this medication.
研究概览
研究类型
观察性的
注册 (实际的)
26
联系人和位置
本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。
学习地点
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North Carolina
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Chapel Hill、North Carolina、美国、27599
- University of North Carolina
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参与标准
研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。
资格标准
适合学习的年龄
18年 至 55年 (成人)
接受健康志愿者
是的
有资格学习的性别
全部
取样方法
非概率样本
研究人群
Neurology/MS clinic: patients with Relapsing Remitting MS "Treatment naïve Relapsing Remitting MS patients will be recruited to provide samples for the in vitro tests.
In addition, Relapsing Remitting MS patients who are already receiving treatment with teriflunomide as a part of their routine care will be recruited to obtain blood samples for the in vivo testing."
描述
Inclusion Criteria:
- confirmed diagnosis of RRMS according to McDonald's diagnostic criteria,
- age 18-55,
- an extended disability status score (EDSS) of 1.5-5.5.
Exclusion Criteria:
- Previous treatment with DMT.
学习计划
本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。
研究是如何设计的?
设计细节
研究衡量的是什么?
主要结果指标
结果测量 |
大体时间 |
|---|---|
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Percent Inhibition of activated/memory B-cells derived from RRMS patients.
大体时间:1 year
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1 year
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次要结果测量
结果测量 |
大体时间 |
|---|---|
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Change in Cytokine Secretion Profile of T-cells stimulated by teriflunomide treatment
大体时间:1 year
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1 year
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Measure the effect of oral teriflunomide on the cytokine secretion as measured in the ex-vivo obtained longitudinal samples from the treated patients.
大体时间:1 year
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1 year
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Measure the effect of oral teriflunomide on the B cell activation as measured in the ex-vivo obtained longitudinal samples from the treated patients.
大体时间:1 year
|
1 year
|
合作者和调查者
在这里您可以找到参与这项研究的人员和组织。
调查人员
- 首席研究员:Silva MarkovicPlese, MD、Universtiy of North Carolina at Chapel Hill
出版物和有用的链接
负责输入研究信息的人员自愿提供这些出版物。这些可能与研究有关。
一般刊物
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研究记录日期
这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。
研究主要日期
学习开始 (实际的)
2016年1月1日
初级完成 (实际的)
2016年12月21日
研究完成 (实际的)
2016年12月21日
研究注册日期
首次提交
2016年6月21日
首先提交符合 QC 标准的
2016年7月12日
首次发布 (估计)
2016年7月14日
研究记录更新
最后更新发布 (实际的)
2017年9月15日
上次提交的符合 QC 标准的更新
2017年9月14日
最后验证
2017年9月1日
更多信息
与本研究相关的术语
其他相关的 MeSH 术语
其他研究编号
- 14-2877
计划个人参与者数据 (IPD)
计划共享个人参与者数据 (IPD)?
未定
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