Pharmaco Kinetic Variability of Infliximab in Rheumatoid Arthritis (FAKIR)
Pharmaco Kinetic and Pharmacokinetic-Pharmacodynamic Variability of Infliximab
Infliximab is a chimeric monoclonal antibody directed towards Tumor Necrosis Factor -alpha that is largely used in inflammatory diseases such as rheumatoid arthritis (RA).
A relationship between dose and clinical outcomes was shown in populations of RA patients but there is an interindividual variability of this relationship. At an individual level, this dose-effet relationship can be separated into the dose-concentration (pharmacokinetic or PK) and the concentration-effet (pharmacokinetic-pharmacodynamic or PK-PD) relationships.
Serum trough concentrations of infliximab have been shown to be variable between patients receiving the same treatment regimen. This PK variability may be explained by several factors (e.g. genetic and immunological factors). The concentration-effect relationship may also be variable and the sources of this variability need to be studied as well. To date no detailed infliximab PK analysis has been published. The sources of variability of the dose-effect relationship need to be characterized to optimize infliximab dosing regimen in patients.
The FAKIR study is a multicenter prospective observational study that will focus on patients treated with infliximab. Its aims are:
- to characterize the PK and PK-PD variability of infliximab in RA, using clinical criteria and biomarkers, assessed over time ;
- to study the influence of the polymorphism of FCGRT (the gene encoding FcRn) on the PK variability of infliximab; to study the influence of the polymorphism of FCGR3A (the gene encoding Fc gamma RIIIa) on the PK-PD variability of infliximab; and to study the influence of antibodies toward infliximab on the PK and PK-PD variabilities of infliximab.
研究概览
研究类型
注册 (实际的)
联系人和位置
学习地点
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Brest、法国
- CHRU de Brest
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Nantes、法国
- CHRU de Nantes
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Orléans、法国
- CHR d'Orléans
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Poitiers、法国
- CHRU de Poitiers
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Rennes、法国
- CHRU de Rennes
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Tours、法国
- CHRU de Tours
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参与标准
资格标准
适合学习的年龄
接受健康志愿者
有资格学习的性别
取样方法
研究人群
描述
Inclusion Criteria:
- Rheumatoid arthritis according to ACR criteria
- Patient already receiving infliximab for more than 14 weeks
- No modification of the dose regimen of infliximab since the last infusion
- No modification of disease modifying anti rheumatic drugs since the last 4 weeks
Exclusion Criteria:
- Surgery scheduled during the duration of the study
- Pregnancy
- infection, malignancy, immune reaction to infliximab or demyelinating diseases
学习计划
研究是如何设计的?
设计细节
队列和干预
团体/队列 |
干预/治疗 |
|---|---|
|
A
Rhumatoid arthritis patient currently receiving infliximab
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chimeric monoclonal antibody to Tumor Necrosis Factor-alpha
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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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Characterizing the PK and PK-PD variability of infliximab in RA
大体时间:6 to 12 weeks
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6 to 12 weeks
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次要结果测量
结果测量 |
大体时间 |
|---|---|
|
Studying the relation between FCGRT polymorphism and the PK variability of infliximab; the relation between FCGR3A polymorphism and the PK-PD variability of infliximab; and the relation between ATI and the PK and PK-PD variabilities of infliximab
大体时间:6 to 12 weeks
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6 to 12 weeks
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合作者和调查者
调查人员
- 首席研究员:Denis MULLEMAN, MD、CHRU de Tours
出版物和有用的链接
研究记录日期
研究主要日期
学习开始
初级完成 (实际的)
研究完成 (实际的)
研究注册日期
首次提交
首先提交符合 QC 标准的
首次发布 (估计)
研究记录更新
最后更新发布 (估计)
上次提交的符合 QC 标准的更新
最后验证
更多信息
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