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Clinical Trials/NCT03604471
NCT03604471CompletedPhase 4

Lipid-lowering Therapy Individualization

Université Catholique de Louvain1 site in 1 country75 target enrollmentStarted: August 8, 2017Last updated:
Conditions
Interventions
Drugs

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

Other

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

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Laure Elens

Professor

Université Catholique de Louvain

Study Sites (1)

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