drugset / Trial / NCT02988115

Evaluation of the Efficacy and Safety of Bempedoic Acid (ETC-1002) in Patients With Hyperlipidemia and Statin Intolerant

NCT02988115 ↗

Phase 3 Completed 345 enrolled Esperion Therapeutics, Inc.
RandomizedParallel-groupTriple-blindTreatment

Summary

The purpose of this study is to determine if bempedoic acid (ETC-1002) is effective and safe versus placebo in patients with elevated LDL cholesterol and who are statin-intolerant.

Timeline

Start
2016-11-16
Primary completion
2018-03-16
Completion
2018-03-16

Outcome

Met primary endpoint

registry analysis (superiority test); Bempedoic Acid vs Placebo; p <0.001; Least squares means difference -21.41 (95% CI -25.132 to -17.697); ANCOVA NCT02988115 ↗

paper Bempedoic acid treatment significantly reduced low-density lipoprotein cholesterol from baseline to week 12 (placebo-corrected difference, -21.4% [95% CI, -25.1% to -17.7%]; P<0.001). PMID 30922146 ↗

release “In Esperion’s CLEAR Serenity trial, bempedoic acid was shown to significantly lower both LDL-cholesterol and high-sensitivity C-reactive protein (hsCRP) in statin-intolerant patients.” esperion.com ↗

release “In the challenging group of patients with statin intolerance, CLEAR Serenity demonstrates that bempedoic acid reduced LDL-cholesterol significantly more than placebo.” esperion.com ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Bempedoic acid Small molecule 180 mg Oral