CI

At a glance

ClinicalIndex Comparison Record
Phase 3Completed· 379 enrolled
Drug / intervention
Epanova +1 moredrug
Likely dose
Epanova 1 gfrom 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/NCT02009865
NCT02009865Phase 3Completed

A 12-Week, Randomized, Double-Blind, Olive Oil-Controlled Phase 3 Study to Assess the Efficacy and Safety of EPANOVA™ in Subjects With Severe Hypertriglyceridemia (EVOLVE II)

AstraZeneca·interventional·Posted Dec 12, 2013·Updated Sep 10, 2019

In Brief

A Phase 3 clinical trial evaluating Epanova and Olive Oil for Hypertriglyceridemia. Completed, enrolled 379 participants across 40 sites in 7 countries.

Detailed Summary

This is a double-blind, randomized, olive oil-controlled study to investigate the efficacy and safety of Epanova as an adjunct therapy to diet for reduction of TG levels in subjects with severe hypertriglyceridemia. The study consists of an approximately 8-week screening period that includes a diet and lifestyle stabilization and washout period and a 12-week treatment period.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesCanada, Czechia, Denmark, Hungary, Netherlands, Russia, United States
Collaborators--

Timeline

Phase 3CompletedFinished
2014201520162017201820192020202120222023202420252026
First PostedDec 12, 2013
Enrollment StartDec 16, 2013
Primary CompletionDec 23, 2014
TodayJul 2, 2026
Enrollment to primary: 1.0 yearsPosted 12.6 years ago

Interventions

Epanovadrug

Epanova will be provided in 1 g polyacrylate-coated soft gel capsules. Two capsules will be taken once per day, without regard to meals, for 12 weeks. At clinic visits, study drug will be administered at the clinic after fasting blood draws are complete.

Olive Oildrug

Olive oil will be provided in 1 g polyacrylate-coated soft gel capsules. Two capsules will be taken once per day, without regard to meals, for 12 weeks. At clinic visits, study drug will be administered at the clinic after fasting blood draws are complete.