Chronic Administration of Anacetrapib Is Associated With Accumulation in Adipose and Slow Elimination

R. Krishna, F. Gheyas, Y. Liu, D. R. Hagen, B. Walker, A. Chawla, J. Cote, R. O. Blaustein, D. E. Gutstein

Research output: Contribution to journalArticlepeer-review

36 Scopus citations

Abstract

Anacetrapib is a novel cholesteryl-ester transfer protein (CETP) inhibitor in late-stage clinical development, shown in preceding clinical trials to have residual pharmacological activity after prolonged washout after chronic dosing. Preclinical findings suggest that white adipose tissue is a potential depot and that accumulation into adipose tissue governs the long-term kinetics of anacetrapib in mice. A phase I study performed to test this hypothesis in humans revealed that plasma exposure was correlated with fat content in food administered with the drug. Plasma concentrations of anacetrapib seemed to reach plateau faster than adipose concentrations. Anacetrapib continued to accumulate in adipose during the treatment period despite apparent plateau in plasma with only minimal decline in adipose levels up to 1 year postdose. Because of its high lipophilicity, anacetrapib partitions into adipose tissue, this likely forms a drug reservoir that, in turn, contributes to the long residence time of the drug in plasma.

Original languageEnglish
Pages (from-to)832-840
Number of pages9
JournalClinical Pharmacology and Therapeutics
Volume102
Issue number5
DOIs
StatePublished - Nov 2017
Externally publishedYes

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