No clinically relevant drug–drug interactions when dalcetrapib is co-administered with atorvastatin

阿托伐他汀 最大值 药理学 加药 医学 药代动力学 胆固醇转移蛋白 内科学 胆固醇 脂蛋白
作者
Michael Derks,Markus Abt,Graeme Parr,Georgina Meneses‐Lorente,Anne-Marie Young,Mary C. Phelan
出处
期刊:Expert Opinion on Investigational Drugs [Taylor & Francis]
卷期号:19 (10): 1135-1145 被引量:17
标识
DOI:10.1517/13543784.2010.509342
摘要

Objectives: Dalcetrapib, which targets cholesteryl ester transfer protein, is in clinical development for prevention of cardiovascular events and is likely to be used concomitantly with statins. Two studies investigated co-administration of dalcetrapib with atorvastatin and any effects of the timing of atorvastatin on the pharmacokinetics of dalcetrapib.Research design and methods: Two crossover studies were performed in healthy subjects: a two-period study of dalcetrapib 900 mg concurrently with atorvastatin (concurrent dosing study) and a three-period study of dalcetrapib 600 mg (dose chosen for Phase III) with atorvastatin concurrently or serially 4 h after dalcetrapib (interval dosing study).Main outcome measures: The primary pharmacokinetic end points were AUC0 – 24 and Cmax; lipid effects and tolerability were secondary end points.Results: In the concurrent study (n = 26), co-administration reduced dalcetrapib AUC0 – 24 and Cmax and caused small changes in AUC0 – 24 and Cmax of atorvastatin and its active metabolites. In the interval study (n = 52), serial and concurrent co-administration of atorvastatin resulted in similar reductions in dalcetrapib exposure that were comparable to those observed in the concurrent dosing study. Co-administration did not decrease the efficacy of dalcetrapib or atorvastatin and was generally well tolerated.Conclusions: These results indicate no clinically relevant interactions for co-administration of dalcetrapib with atorvastatin.

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