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临床试验/NCT03604471
NCT03604471已完成4 期

Lipid-lowering Therapy Individualization

Université Catholique de Louvain1 个研究点 分布在 1 个国家目标入组 75 人开始时间: 2017年8月8日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
4 期
状态
已完成
入组人数
75
试验地点
1
主要终点
Atorvastatin metabolites population pharmacokinetics

研究概览

简要总结

This clinical study will explore individual factors influencing statin pharmacokinetics in a cohort of 150 patients treated with atorvastatin.

详细描述

Atorvastatin is widely prescribed for the treatment of hypercholesterolemia to prevent the risk of cardiovascular diseases, a leading death cause in industrialized countries. There exists considerable inter-individual variability in response to statins, reflected by differences in lipid-lowering effect or risk of presenting adverse drug reaction; mainly myotoxicity. A plethora of different factors (demographic, genetic, physiopathologic, environmental...) have been tested to explain this variability but it lacks of pharmacokinetic (PK) data and/or replications of observations are rare and results remain inconclusive, probably because of non-adapted designs and no-clear driven-hypothesis but also due to a lack of scientific rationale and deep mechanistic understanding. This clinical study will explore individual factors influencing statin PK in a cohort of 150 patients treated with atorvastatin. The collection of meticulous clinical PK data and a rigorous statistical analysis will allow quantifying the effect of each identified parameter on statin PK and eventually, defining a population-based PK model taking into account the combined effect of all covariates in a quantitative approach. This innovative prospectively designed clinical study will ultimately allow predicting atorvastatin PK fluctuations and anticipating any inadequate dosing in clinical care.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Other
盲法
None

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

  • Treatment with atorvastatin (any dose)

排除标准

  • Unable to provide informed consent

研究组 & 干预措施

Atorvastatin

Other

All patients using atorvastatin at any dose (usually ranging from 5 to 80 mg once-daily).

干预措施: Atorvastatin (Drug)

结局指标

主要结局

Atorvastatin metabolites population pharmacokinetics

时间窗: 18 months

Concentrations of ortho-hydroxyatorvastatin (pmol/ml), para-hydroxyatorvastatin (pmol/ml) and atorvastatin lactone (pmol/ml) will be measured by HPLC-MS using sparse samples obtained over the entire study period. Data will be pooled and analyzed using population pharmacokinetic modeling. The reported pharmacokinetic parameters will depend on the type of model that best fits the data.

Atorvastatin population pharmacokinetics

时间窗: 18 months

Concentrations of atorvastatin acid (pmol/ml) will be measured by HPLC-MS using sparse samples obtained over the entire study period. Data will be pooled and analyzed using population pharmacokinetic modeling. The reported pharmacokinetic parameters will depend on the type of model that best fits the data.

次要结局

  • Triglycerides(18 months)
  • Creatine kinase(18 months)
  • Pharmacogene genotype(18 months)
  • Cholesterol(18 months)
  • Occurrence of adverse drug events(18 months)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Laure Elens

Professor

Université Catholique de Louvain

研究点 (1)

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