Evacetrapib
In Japanese patients, evacetrapib added to atorvastatin cuts LDL-C by 25.70% versus placebo and more than doubles HDL-C (Circ J 2017)
Original title: Efficacy and Safety of the Cholesteryl Ester Transfer Protein Inhibitor Evacetrapib in Combination With Atorvastatin in Japanese Patients With Primary Hypercholesterolemia
This multicenter, randomized, 12-week, double-blind, placebo-controlled phase 3 study tested evacetrapib added to atorvastatin in 149 Japanese patients with primary hypercholesterolemia, randomized to evacetrapib plus atorvastatin (n=53), ezetimibe plus atorvastatin (n=50), or placebo plus atorvastatin (n=46). Evacetrapib 130 mg daily for 12 weeks produced a statistically significant treatment difference of -25.70% in LDL-C versus placebo (95% CI -34.73 to -16.68, P less than 0.001) and a statistically significant 126.39% difference in HDL-C change versus placebo (95% CI 113.54-139.24, P less than 0.001). No deaths or serious adverse events occurred, with four patients discontinuing due to adverse events (three on evacetrapib, one on ezetimibe), confirming evacetrapib with atorvastatin was superior to placebo for LDL-C lowering and HDL-C raising with no new safety concerns identified.
Original abstract
Background: Inhibition of cholesteryl ester transfer protein by evacetrapib when added to atorvastatin may provide an additional treatment option for patients who do not reach their low-density lipoprotein cholesterol (LDL-C) goal.
Methods And Results: This multicenter, randomized, 12-week, double-blind, parallel-group, placebo-controlled, outpatient, phase 3 study evaluated the efficacy of evacetrapib with atorvastatin in reducing LDL-C in 149 Japanese patients (evacetrapib/atorvastatin, n=53; ezetimibe/atorvastatin, n=50; placebo/atorvastatin, n=46) with primary hypercholesterolemia. The primary efficacy measure was percent change from baseline to week 12 in LDL-C (β quantification). Treatment with evacetrapib 130 mg daily for 12 weeks resulted in a statistically significant treatment difference of -25.70% compared with placebo in percentage decrease in LDL-C (95% CI: -34.73 to -16.68; P<0.001). Treatment with evacetrapib 130 mg also resulted in a statistically significant difference of 126.39% in the change in high-density lipoprotein cholesterol (HDL-C) compared with placebo (95% CI: 113.54-139.24; P<0.001). No deaths or serious adverse events were reported. Four patients (3 in the evacetrapib group and 1 in the ezetimibe group) discontinued due to adverse events.
Conclusions: Evacetrapib daily in combination with atorvastatin was superior to placebo in lowering LDL-C after 12 weeks, and resulted in a statistically significant increase of HDL-C compared with placebo. Also, no new safety risks were identified.
ancestryevacetrapiboutcomes trials
Summary written by cetpinhibition.org from the published abstract; figures as published. Page updated 18 August 2026. Methods.