Lipid-lowering Therapy Individualization
Trial Snapshot
- Phase
- Phase 4
- Status
- Completed
- Enrollment
- 75
- Locations
- 1
- Primary Endpoint
- Atorvastatin metabolites population pharmacokinetics
Study Overview
Brief Summary
This clinical study will explore individual factors influencing statin pharmacokinetics in a cohort of 150 patients treated with atorvastatin.
Detailed Description
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.
Study Design
- Study Type
- Interventional
- Allocation
- Na
- Intervention Model
- Single Group
- Primary Purpose
- Other
- Masking
- None
Eligibility Criteria
- Ages
- 18 Years to — (Adult, Older Adult)
- Sex
- All
- Accepts Healthy Volunteers
- No
Inclusion Criteria
- •Treatment with atorvastatin (any dose)
Exclusion Criteria
- •Unable to provide informed consent
Arms & Interventions
Atorvastatin
All patients using atorvastatin at any dose (usually ranging from 5 to 80 mg once-daily).
Intervention: Atorvastatin (Drug)
Outcomes
Primary Outcomes
Atorvastatin metabolites population pharmacokinetics
Time Frame: 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
Time Frame: 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.
Secondary Outcomes
- Triglycerides(18 months)
- Creatine kinase(18 months)
- Pharmacogene genotype(18 months)
- Cholesterol(18 months)
- Occurrence of adverse drug events(18 months)
Investigators
Laure Elens
Professor
Université Catholique de Louvain
