CI

At a glance

ClinicalIndex Comparison Record
Phase 3Completed· 138 enrolled
Drug / intervention
ezetimibe +1 moredrug
Likely dose
ezetimibe 10 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/NCT00867165
NCT00867165Phase 3Completed

A Randomized, Double-Blind, Parallel-Group, Placebo-Controlled Efficacy and Safety Study of Ezetimibe Monotherapy in Children (Ages 6 to 10 Years) With Primary Hypercholesterolemia (Heterozygous Familial and Nonfamilial) (Phase 3, Protocol No. P05522)

Organon and Co·interventional·Posted Mar 23, 2009·Updated May 21, 2024

In Brief

A Phase 3 clinical trial evaluating ezetimibe and Placebo for Primary Hypercholesterolemia. Completed, enrolled 138 participants.

Detailed Summary

The purpose of this study is to determine the effect of ezetimibe 10 mg/day compared to placebo on the reduction of low-density lipoprotein cholesterol (LDL-C) from baseline to 12 weeks of treatment in children \>=6 to \<=10 years old with primary hypercholesterolemia. The study will also evaluate the effect of ezetimibe on total cholesterol (TC), apolipoprotein B (Apo B), high-density lipoprotein cholesterol (HDL-C), non-HDL-C, and triglycerides (TG). The safety of ezetimibe in this subject population will also be evaluated.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
Countries--

Timeline

Phase 3CompletedFinished
200920102011201220132014201520162017201820192020202120222023202420252026
First PostedMar 23, 2009
Enrollment StartMay 21, 2009
Primary CompletionApr 13, 2012
TodayJul 2, 2026
Enrollment to primary: 2.9 yearsPosted 17.3 years ago

Interventions

ezetimibedrug

oral tablets: ezetimibe 10 mg once daily for 12 weeks

Placebodrug

oral tablets: placebo to match ezetimibe 10 mg; administered once daily during the 5-week, single-blind, placebo run-in and diet stabilization period and 12-week double-blind treatment period