drugset / Trial / NCT03337308

A Study Evaluating the Safety and Efficacy of Bempedoic Acid Plus Ezetimibe Fixed-Dose Combination Compared to Bempedoic Acid, Ezetimibe, and Placebo in Patients Treated With Maximally Tolerated Statin Therapy

NCT03337308 ↗

Phase 3 Completed 382 enrolled Esperion Therapeutics, Inc.
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The purpose of this study is to determine if Bempedoic Acid (BA) + Ezetimibe (EZE) in a fixed-dose combination (FDC) is effective and safe versus its individual components and placebo in patients with elevated LDL cholesterol treated with maximally tolerated statin therapy.

Timeline

Start
2017-10-23
Primary completion
2018-06-18
Completion
2018-07-18

Outcome

Met primary endpoint

registry analysis (superiority test); Bempedoic Acid 180 mg + Ezetimibe 10 mg FDC vs Placebo; p <0.001; Difference of Least Squares (LS) means -38.0 (95% CI -46.5 to -29.6); ANCOVA NCT03337308 ↗

paper At week 12, the fixed-dose combination lowered low-density lipoprotein cholesterol (-36.2%) significantly more than placebo (1.8% PMID 31357887 ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Bempedoic acid Small molecule 180 mg Oral
Comparator Ezetimibe Unknown 10 mg Oral

Indications