Dalcetrapib
Atorvastatin reduces exposure to dalcetrapib without diminishing its cardiovascular benefit, two crossover studies find (Expert Opin Investig Drugs 2010)
Original title: No clinically relevant drug-drug interactions when dalcetrapib is co-administered with atorvastatin
Two crossover studies in healthy subjects examined co-administration of dalcetrapib with atorvastatin: a two-period study of dalcetrapib 900 mg given concurrently with atorvastatin, and a three-period study of dalcetrapib 600 mg, the phase III dose, given concurrently or 4 hours after atorvastatin. In the concurrent study (n=26), co-administration reduced dalcetrapib AUC and Cmax and caused small changes in atorvastatin and its active metabolites. In the interval study (n=52), serial and concurrent dosing produced similar reductions in dalcetrapib exposure, comparable to the concurrent dosing study. Co-administration did not decrease the efficacy of either dalcetrapib or atorvastatin and was generally well tolerated, indicating no clinically relevant interaction.
Original abstract
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 AUC(0 - 24) and C(max); lipid effects and tolerability were secondary end points.
Results: In the concurrent study (n = 26), co-administration reduced dalcetrapib AUC(0 - 24) and C(max) and caused small changes in AUC(0 - 24) and C(max) 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.
dalcetrapibpharmacologystatins
Summary written by cetpinhibition.org from the published abstract; figures as published. Page updated 18 August 2026. Methods.