drugset / Trial / NCT04239950
Efficacy of Ethyl Icosapentate in Patients With Severe Hypertriglyceridemia
Phase 3
Completed
316 enrolled
Mochida Pharmaceutical Company, Ltd.
Marubeni Pharmaceuticals (Suzhou) Co., Ltd. · collab
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
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | icosapent ethyl | Small molecule | 0.9 g | Oral |
| Subject | icosapent ethyl | Small molecule | 1.8 g | Oral |