drugset / Trial / NCT04239950

Efficacy of Ethyl Icosapentate in Patients With Severe Hypertriglyceridemia

NCT04239950 ↗

RandomizedParallel-groupQuadruple-blindTreatment

Summary

The purpose of this study is to evaluate the efficacy and safety of ethyl icosapentate in Chinese patients with severe hypertriglyceridemia.

Timeline

Start
2020-05-09
Primary completion
2023-07-20
Completion
2023-07-20

Outcome

Met primary endpoint

paper The MND-21 3600 mg group exhibited a significantly greater reduction in TG levels compared with the placebo group (P = .049). PMID 41500861 ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject icosapent ethyl Small molecule 0.9 g Oral
Subject icosapent ethyl Small molecule 1.8 g Oral

Indications