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Clinical Trial Summary

The goal of this study is to evaluate the efficacy, safety, and tolerability of MK-0616 in adult participants with hypercholesterolemia. The primary hypothesis is that MK-0616 is superior to placebo on mean percent change from baseline in low-density lipoprotein cholesterol (LDL-C) at Week 24.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05952856
Study type Interventional
Source Merck Sharp & Dohme LLC
Contact
Status Active, not recruiting
Phase Phase 3
Start date August 10, 2023
Completion date September 24, 2025

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