Dalcetrapib
Torcetrapib can double HDL cholesterol while lowering LDL cholesterol by up to 42 percent, a review of CETP inhibitors reports (Curr Opin Pharmacol 2006)
Original title: Raising high-density lipoprotein with cholesteryl ester transfer protein inhibitors
This review traces the search for synthetic CETP inhibitors over the preceding 15 years, motivated by the reciprocal rise in HDL cholesterol and fall in LDL cholesterol seen with CETP deficiency. Two potent inhibitors, JTT-705 and torcetrapib, were then undergoing clinical trials. The review highlights recent reports that torcetrapib can simultaneously raise HDL cholesterol twofold and lower LDL cholesterol by up to 42%, findings that heightened interest in the CETP-inhibitor class. Upcoming phase III trial results for torcetrapib were expected to provide anatomical measurements of atherosclerosis, offering the first direct assessment of therapeutic benefit from CETP inhibition.
Original abstract
Cholesteryl ester transfer protein (CETP) catalyzes the transfer of cholesteryl ester from high-density lipoprotein (HDL) to apolipoprotein B-containing lipoproteins in exchange for triglyceride, and thereby plays a major role in lipoprotein metabolism. The reciprocal increase in HDL cholesterol (HDL-C) and decrease in low-density lipoprotein cholesterol (LDL-C) associated with CETP deficiency has led to the search for synthetic CETP inhibitors over the past 15 years. Several potent inhibitors have been identified, two of which--JTT-705 and torcetrapib--are undergoing clinical trials. Recent reports that torcetrapib is able to simultaneously raise HDL-C twofold and lower LDL-C by < or = 42% has heightened interest in this new class of agents. Upcoming results from Phase III trials of torcetrapib should provide anatomical measurements of atherosclerosis and thus the first assessment of therapeutic benefit.
dalcetrapibHDL biologytorcetrapib
Summary written by cetpinhibition.org from the published abstract; figures as published. Page updated 18 August 2026. Methods.