The purpose of this study is to evaluate the efficacy and safety of MK-0616, an oral PCSK9 inhibitor, in lowering low-density lipoprotein cholesterol (LDL-C) in participants with hypercholesterolemia. The primary hypothesis is that at least one of the four doses of MK-0616 tested in this study is superior to placebo on percent change from baseline in LDL-C at Week 8.
| Condition | Hypercholesterolemia, Familial Hypercholesterolemia |
|---|---|
| Treatment | Placebo, MK-0616 |
| Clinical Study Identifier | NCT05261126 |
| Sponsor | Merck Sharp & Dohme LLC |
| Last Modified on | 8 August 2022 |
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