Key result
Obicetrapib triple therapy regresses pre-existing atherosclerotic lesions by ~44% in mice.
Why the study?
Does obicetrapib alone or combined with ezetimibe and atorvastatin reduce non-HDL-C and regress atherosclerosis in APOE*3-Leiden.CETP mice?
Does obicetrapib alone or combined with ezetimibe and atorvastatin reduce non-HDL-C and regress atherosclerosis in APOE*3-Leiden.CETP mice?
Answers are grounded in this paper and cite their sources.
In a mouse model, obicetrapib combined with ezetimibe and atorvastatin synergistically lowers non-HDL-C and promotes regression of established atherosclerosis.
The selective cholesteryl ester transfer protein (CETP) inhibitor obicetrapib is in clinical evaluation for dyslipidemia and cardiovascular risk reduction. This study investigated how obicetrapib alone and with ezetimibe reduces non-HDL-C, affects atherosclerotic lesion progression, and regression when added to background atorvastatin intervention. APOE*3-Leiden.CETP mice received a Western-type diet (WTD) or this diet supplemented with obicetrapib, ezetimibe or both. After 8 weeks, all interventions reduced non-HDL-C levels (obicetrapib: -53%; ezetimibe: -19%; combination: -75%). Obicetrapib mono and combination treatment blocked CETP activity (-99% and -98%), thereby increasing HDL-C levels (+286% and +256%). Very low-density lipoprotein (VLDL) cholesterol production was not affected, while obicetrapib and the combination with ezetimibe increased VLDL clearance (plasma half-life [¹⁴C]-cholesteryloleate: -44% and -57%) and LDL receptor expression (+63% and +74%), without increasing liver lipids. Atherosclerosis progression was evaluated after 28 weeks. All interventions reduced atherosclerotic lesion area (obicetrapib: -90%; ezetimibe: -50%; combination: -98%) and severity due to almost complete reductions in severe lesions (obicetrapib: -80%; combination: -98%). Non-HDL-C exposure (p<0.001) was independently associated with lesion area, in contrast to HDL-C (p=0.336). Combination treatment synergistically reduced non-HDL-C and atherosclerosis. For atherosclerosis regression, mice with advanced and established atherosclerosis received obicetrapib and ezetimibe on top of atorvastatin for 24 weeks. Triple therapy regressed lesion area (-44% versus baseline) and increased healthy vessel segments, indicating potential for complete atherosclerosis resolution. In summary, obicetrapib alone and with ezetimibe reduces non-HDL-C by enhancing LDL receptor-mediated VLDL clearance, thereby synergistically reducing atherosclerosis. Triple treatment with obicetrapib, ezetimibe and atorvastatin regresses pre-existent atherosclerotic lesions.
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Inia et al. (2026) studied Dyslipidemia and atherosclerosis. Obicetrapib alone or with ezetimibe (and atorvastatin) vs. Western-type diet (WTD) alone or baseline was evaluated on Non-HDL-C levels and atherosclerotic lesion area. In APOE*3-Leiden.CETP mice, obicetrapib alone and with ezetimibe reduced non-HDL-C and atherosclerotic lesion area, and triple therapy with atorvastatin regressed pre-existent lesions by 44%.
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