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Clinical Trial Summary

This is a randomized, double-blind, multi-center, therapeutic confirmatory, phase 3 trial to evaluate the efficacy and safety of CKD-391 and CKD-331 in patients with primary hypercholesterolemia


Clinical Trial Description

Participants were randomly assigned in a 1:1:1:1 ratio to the following groups: combination therapy of D377 and CKD-331, D377, CKD-331, and D086. The patients are prescribed oral administration of the appropriate IP daily (3 tablets: actual medication and placebo) for 8 weeks. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05657574
Study type Interventional
Source Chong Kun Dang Pharmaceutical
Contact SeungHwan Lee, MD
Phone +82-2-3010-4829
Email seungwlee@amc.seoul.kr
Status Recruiting
Phase Phase 3
Start date November 24, 2022
Completion date June 2023

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