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Clinical Trial Summary

The primary objective was to investigate the effect of 12-week treatment of Omacor on fasting serum triglycerides (TG) in Chinese subjects with hypertriglyceridemia (HTG). The secondary objectives were to investigate the safety and tolerability and effect of Omacor on lipid parameters after 12 weeks treatment.


Clinical Trial Description

This was a multicenter, randomized, double-blind, parallel-group study of twice daily treatment of Omacor or matching placebo in subjects with moderate or severe HTG. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04756180
Study type Interventional
Source Abbott
Contact
Status Completed
Phase Phase 3
Start date October 2016
Completion date April 2019

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