Abstract
By virtue of their effects on low-density lipoprotein cholesterol, high-density lipoprotein cholesterol, and cellular cholesterol efflux, there is considerable interest in the potential use of pharmacological inhibitors of cholesteryl ester transfer protein (CETP) as a novel approach for cardiovascular disease prevention. This is supported by observations from genetic and animal studies suggesting that less CETP activity has favorable cardiovascular effects. Despite the adverse effects of the first CETP inhibitor to move forward in clinical development, torcetrapib, there remains considerable interest in developing alternative CETP inhibitors without the off-target effects of torcetrapib. The clinical development programs leading to a number of promising CETP inhibitors will be reviewed.
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Stephen J. Nicholls reports receiving research support from AstraZeneca, Amgen, Eli Lilly, Novartis, Resverlogix, Sanofi-Regeneron, Anthera, and Cerenis and is a consultant for AstraZeneca, Amgen, Boehringer Ingelheim, CSL Behring, Eli Lilly, Merck, Takeda, Roche, Novartis, and Sanofi-Regeneron.
Kohei Takata reports grants from the Clinical Research Promotion Foundation.
Belinda Di Bartolo and MyNgan Duong declare that they have no conflict of interest.
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This article does not contain any studies with human or animal subjects performed by any of the authors.
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This article is part of the Topical Collection on Lipid Abnormalities and Cardiovascular Prevention
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Di Bartolo, B., Takata, K., Duong, M. et al. CETP Inhibition in CVD Prevention: an Actual Appraisal. Curr Cardiol Rep 18, 43 (2016). https://doi.org/10.1007/s11886-016-0724-y
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DOI: https://doi.org/10.1007/s11886-016-0724-y