CI

At a glance

ClinicalIndex Comparison Record
Phase 3Completed· 575 enrolled
Drug / intervention
Fixed Combination of Fenofibrate/simvastatin 145/20 mg +4 moredrug
Likely dose
Fixed Combination of Fenofibrate/simvastatin 145/20 mgfrom record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT01674712
NCT01674712Phase 3Completed

A 12-week, Double-blind, Randomized Study to Compare the Efficacy and Safety of Fixed Combinations of Fenofibrate / Simvastatin 145/20mg and Fenofibrate / Simvastatin 145/40mg Tablets vs. Matching Monotherapies in Dyslipidemic Subjects at High Risk of Cardiovascular Disease.

Abbott·interventional·Posted Aug 29, 2012·Updated Dec 11, 2014

In Brief

A Phase 3 clinical trial evaluating Fixed Combination of Fenofibrate/simvastatin 145/20 mg, Simvastatin 20 mg, and 3 other interventions for Dyslipidemia. Completed, enrolled 575 participants across 69 sites in 7 countries.

Detailed Summary

This is a double-blind, randomized study designed to compare the efficacy and safety of two fixed combinations of fenofibrate / simvastatin 145/20 mg and fenofibrate / simvastatin 145/40 mg tablets vs. matching monotherapies in subjects with abnormal fat (lipids) in the blood and at high risk of cardiovascular disease. Fenofibrate is a treatment that lowers fat in blood. It is prescribed in patients with high levels of triglycerides (TG). The drug has been marketed in more than 80 countries since 1975. Simvastatin is also used for the treatment of patients with a high level of cholesterol. These have also been marketed worldwide for more than 20 years. It is important to treat high levels of fats in the blood because it has been shown that even mildly elevated level of lipids in the blood can lead to diseases of the blood vessels. It has been shown in several studies and in clinical practice that the combination of fenofibrate plus simvastatin can lead to improved effects on blood fats, compared to treatment with simvastatin or fenofibrate alone. The main objective of the study is to compare the efficacy of the two fixed-combinations (FC) -fenofibrate/simvastatin 145/20 mg tablet and fenofibrate/simvastatin 145/40 mg tablet in reducing TG and increasing high density lipoprotein cholesterol (HDL-C) versus simvastatin 20 mg or 40 mg, and in reducing low density lipoprotein cholesterol (LDL-C) versus fenofibrate 145 mg.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsDyslipidemia
CountriesArgentina, Czechia, Germany, Mexico, Poland, Romania, Russia
Collaborators--

Timeline

Phase 3CompletedFinished
20132014201520162017201820192020202120222023202420252026
First PostedAug 29, 2012
Enrollment StartJun 1, 2012
Primary CompletionOct 1, 2013
TodayJul 2, 2026
Enrollment to primary: 1.3 yearsPosted 13.8 years ago

Interventions

Fixed Combination of Fenofibrate/simvastatin 145/20 mgdrug

Fenofibrate/simvastatin oval biconvex film-coated tablet, 145 mg / 20 mg, once daily, 12 weeks

Simvastatin 20 mgdrug

Simvastatin generic tablet over-encapsulated, 20 mg, once daily, 12 weeks

Fenofibrate 145 mgdrug

Fenofibrate, tablet, 145 mg, once daily, 12 weeks

Fixed Combination of Fenofibrate/simvastatin 145/40 mgdrug

Fenofibrate/simvastatin film-coated tablet 145 mg / 40 mg, once daily, 12 weeks

Simvastatin 40 mgdrug

simvastatin, generic tablet over-encapsulated, 40 mg, once daily, 12 weeks