Effect of Renal Impairment on the Pharmacokinetics of Cilostazol and its Metabolites

Abstract

Objective

The pharmacokinetics of cilostazol were studied in patients with mild, moderate and severe renal impairment and in healthy volunteers after administration of 50mg single and multiple doses of cilostazol.

Design

This was an open-label, single and multiple dose study administering 50mg cilostazol every 12 hours to healthy volunteers and patients with varying degrees of renal impairment.

Participants

6 normal volunteers [creatinine clearance (CL^CR) ≥90 ml/min]; 6 patients with mild (CL^CR 50 to 89 ml/min), 5 with moderate (CL^CR 26 to 49 ml/min) and 6 with severe (CL^CR 5 to 25 ml/min) renal impairment.

Outcome Measures

Noncompartmental pharmacokinetic parameters were determined for each study participant.

Results

At steady state, in the severe renal disease group, cilostazol and OPC-13015 peak concentrations (C_max) were 29 and 41% lower and the areas under the concentration-time curve over the dosage interval (AUC_τ) 39 and 47% lower than in the healthy volunteers. C_max and AUC_τ of OPC-13213 were significantly higher, 173 and 209%, respectively, than those in the healthy volunteers. The accumulation ratios were not significantly different between the various renal function groups for cilostazol and its metabolites. The estimated pharmacological activity of cilostazol and its metabolites was similar between the normal volunteers and those with severe renal impairment.

Conclusions

A dosage reduction in renally impaired patients is not supported by the pharmacokinetics of cilostazol and its metabolites in this patient group.