Clinical Trials Directory

Trials / Completed

CompletedNCT00117494

Rosuvastatin Versus Pravastatin in HIV Patients Treated With Boosted Protease Inhibitors (PI) (ANRS126)

Randomised Comparative Study of the Efficacy and Safety of Rosuvastatin and Pravastatin in Dyslipidemic Patients Treated With Antiretroviral Agents. Anrs 126

Status
Completed
Phase
Phase 4
Study type
Interventional
Enrollment
86 (planned)
Sponsor
French National Agency for Research on AIDS and Viral Hepatitis · Other Government
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

In HIV hypercholesterolemic patients treated with protease inhibitors, some drugs of the statin group are used to control cholesterol level. New and potentially more efficient statins may interfere with protease inhibitors and hence loose a part of their activity. They have thus to be compared with a more established drug of the same class (e.g. pravastatin). The protocol compares the efficacy and safety of rosuvastatin and pravastatin.

Detailed description

The study compares the efficacy and safety of rosuvastatin and pravastatin among dyslipidemic HIV-seropositive patients treated with antiretroviral agents including a boosted protease inhibitor. It is an open, multicenter, randomised trial, with two parallel groups comparing rosuvastatin with pravastatin. Statins are administered from D0, with a single daily dose in the morning, for 45 consecutive days. The duration of the study for each patient will be 45 days not including the preselection period (maximum 15 days). The primary end-point compares the change in LDL cholesterol between D0 and D45, in patients receiving rosuvastatin (10 mg/day) or pravastatin (40 mg/day) and treated by antiretroviral agents including a boosted Protease Inhibitor. Secondary end-points compares changes in triglycerides and HDL cholesterol; percentage of patients with a normal value of LDL cholesterol, HDL cholesterol and triglycerides on D45; clinical safety and laboratory safety parameters of rosuvastatin and pravastatin; distribution profile of the diameter of LDL cholesterol particles. Cmin of rosuvastatin, pravastatin and protease inhibitors (PI) are controlled at D15 for statins and PI.

Conditions

Interventions

TypeNameDescription
DRUGPravastatin
DRUGRosuvastatin

Timeline

Start date
2005-10-01
Primary completion
2007-03-01
Completion
2007-06-01
First posted
2005-07-07
Last updated
2026-04-03

Locations

1 site across 1 country: France

Source: ClinicalTrials.gov record NCT00117494. Inclusion in this directory is not an endorsement.