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PHARMACOKINETICS AND PHARMACODYNAMICS |
From Early Development and Clinical Pharmacology (Dr Katz, Dr Udata, Ms Ott, Ms Hickey, Dr Meng), Biomarker Laboratory, Clinical Translational Medicine (Dr Burczynski, Dr Vesterqvist), and Bioanalytical R&D/Drug Metabolism (Mr Burghart), Wyeth Pharmaceuticals, Collegeville, Pennsylvania.
Liver X-receptor (LXR) agonists have been postulated to enhance reverse cholesterol transport (RCT), a process believed to shuttle cholesterol from the periphery back to the liver. Enhancing RCT via the upregulation of cholesterol transporters such as the adenosine triphosphate-binding cassettes ABCA1 and ABCG1 could therefore inhibit the progression of atherosclerosis. LXR-623 is a synthetic ligand for LXRs
and β that has shown promise in animal models of atherosclerosis. The authors present results from a single ascending-dose study of the safety, pharmacokinetics, and pharmacodynamics of LXR-623 in healthy participants. LXR-623 was absorbed rapidly with peak concentrations (Cmax) achieved at approximately 2 hours. The Cmax and area under the concentration-time curve increased in a dose-proportional manner. The mean terminal disposition half-life was between 41 and 43 hours independently of dose. LXR activation resulted in a dose-dependent increase in ABCA1 and ABCG1 expression. The effect of LXR-623 concentration on ABCA1 and ABCG1 expression was further characterized via a population pharmacokinetic-pharmacodynamic analysis, yielding EC50 estimates of 526 ng/mL and 729 ng/mL, respectively. Central nervous system-related adverse events were observed at the 2 top doses tested. The pharmacodynamic effects described here are the first demonstration of "target engagement" by an LXR agonist in humans.
Key Words: Liver X-receptor (LXR) reverse cholesterol transport (RCT) ATP-binding cassettes ABCA1 ABCG1 population pharmacokinetics and pharmacodynamics
Address for reprints: Arie Katz, MD, 500 Arcola Road, A-3, Collegeville, PA 19426; e-mail: katza2{at}wyeth.com.
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