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Multiple-dose study of the CETP inhibitor CP-800,569 shows dose-dependent HDL rise and LDL fall (Clin Pharmacol Ther 2009)

Original title: Pharmacokinetic, pharmacodynamic, and safety profile of a new cholesteryl ester transfer protein inhibitor in healthy human subjects

Clin Pharmacol Ther · · 6

Wolk R, Chen D, Clark RW, Mancuso J, Barclay PL

Healthy subjects received the new CETP inhibitor CP-800,569 once daily for 14 days at doses of 30 to 1,800 mg. Serum drug levels rose and CETP activity fell in a dose-related manner, with HDL cholesterol rising by a maximum of 156% and LDL cholesterol falling by a maximum of 47%, alongside lowered postprandial triglycerides. Trough apolipoprotein E rose by a maximum of 89% for total plasma apoE and 280% for HDL apoE, while postprandial increases in total and non-HDL apoE were diminished or reversed to decreases. CP-800,569 was very well tolerated, with nonserious gastrointestinal adverse events seen only at 1,800 mg and no changes in blood pressure, though effects on aldosterone and cortisol at higher doses could not be excluded.

Read the paper (DOI)PubMed

Original abstract

A new cholesteryl ester (CE) transfer protein (CETP) inhibitor (CP-800,569) was evaluated. Doses of 30-1,800 mg were administered once daily to healthy subjects for 14 days. Serum CP-800,569 levels increased, and CETP activity decreased, in a dose-related manner. Serum levels of high-density lipoprotein (HDL) increased (by a maximum of 156%), and those of low-density lipoprotein (LDL) decreased (by a maximum of 47%). CP-800,569 also had the effect of lowering postprandial triglyceride levels. Trough concentrations of apolipoprotein E (apoE) increased: the maximum increases were 89% for total plasma apoE and 280% for HDL apoE. By contrast, the postprandial increases in total plasma levels of apoE and non HDL apoE were either diminished by CP-800,569 or reversed to decreases. CP-800,569 was very well tolerated, with some nonserious gastrointestinal adverse events seen only with the 1,800-mg dose. No changes in blood pressure (BP) were observed. The possible effects of higher CP-800,569 doses on aldosterone and cortisol levels could not be excluded. The results of this study may be useful in CP-800,569 dose selection.

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Summary written by cetpinhibition.org from the published abstract; figures as published. Page updated 19 August 2026. Methods.