drugset / Trial / NCT01047683

Efficacy and Safety of AMR101 (Ethyl Icosapentate) in Patients With Fasting Triglyceride (Tg) Levels ≥ 500 and ≤ 2000 mg/dL

NCT01047683 ↗

Phase 3 Completed 229 enrolled Amarin Pharma Inc.
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The primary objective is to determine the efficacy of AMR101 (ethyl icosapentate) compared to placebo in lowering fasting triglyceride levels in patients with very high fasting triglyceride levels ≥ 500 and ≤ 2000 mg/dL.

Timeline

Start
2009-12
Primary completion
2010-10
Completion
2011-07

Outcome

Met primary endpoint

registry analysis (unspecified test); AMR101 (Ethyl Icosapentate) - 4 g/Day vs Placebo; p <0.0001; Median Difference (Final Values) -33.1 (95% CI -46.6 to -21.5); Wilcoxon rank-sum test NCT01047683 ↗

registry analysis (unspecified test); AMR101 (Ethyl Icosapentate) - 2 g/Day vs Placebo; p = 0.0051; Median Difference (Final Values) -19.7 (95% CI -33.3 to -5.6); Wilcoxon rank-sum test NCT01047683 ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject icosapent ethyl Small molecule 2 g —
Subject icosapent ethyl Small molecule 4 g —

Indications