Pharmacokinetic Drug-Drug Interaction between Cilostazol and Rosuvastatin in Healthy Participants

被引:0
|
作者
Kim, Dong Ho [1 ,2 ]
Hong, Jang Hee [1 ,3 ]
Jung, Won Tae [4 ]
Nam, Kyu-Yeol [4 ]
Roh, Jae Seok [4 ]
Lee, Hye Jung [5 ]
Moon, JungHa [5 ]
Kim, Kyu Yeon [5 ]
Jung, Jin-Gyu [6 ]
Sunwoo, Jung [1 ]
机构
[1] Chungnam Natl Univ Hosp, Clin Trials Ctr, 266 Munhwa Ro, Daejeon, South Korea
[2] Chungnam Natl Univ, Coll Med, Dept Med Sci, Daejeon, South Korea
[3] Chungnam Natl Univ, Coll Med, Dept Pharmacol, Daejeon, South Korea
[4] Korea United Pharmaceut Corp, Seoul, South Korea
[5] Caleb Multilab Inc, Seoul, South Korea
[6] Chungnam Natl Univ Hosp, Dept Family Med, 266 Munhwa Ro, Daejeon, South Korea
关键词
FORMULATIONS; ATORVASTATIN; CHOLESTEROL;
D O I
10.1007/s40256-024-00686-w
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background and ObjectivesCilostazol improves ischemic symptoms and prevents recurrence following cerebral infarction, and rosuvastatin reduces cholesterol levels. However, no reports exist on the pharmacokinetic interactions between these two drugs in healthy adults. This study evaluated the pharmacokinetic (PK) interactions and safety of cilostazol and rosuvastatin when co-administered to healthy male participants.MethodsA randomized, open-label, multiple-dosing, two-arm, two-period study was conducted. Arm A had 30 participants receiving 200 mg cilostazol daily and arm B had 27 participants receiving 20 mg rosuvastatin daily for 7 days. In period 2, both arms received a combination of 200 mg cilostazol and 20 mg rosuvastatin daily for 7 days following a 7-day washout period. Plasma concentrations of cilostazol, its metabolites, and rosuvastatin were quantified using liquid chromatography-tandem mass spectrometry.ResultsFifty-seven participants were randomized, and 44 completed the study. The geometric mean ratio (GMR) and 90% confidence intervals (CI) for maximum plasma concentration at steady state (Cmax,ss) and area under the plasma concentration-time curve during the dosing interval at steady state (AUCtau,ss) indicated no significant interaction between cilostazol and rosuvastatin. Safety assessments showed comparable profiles to individual drug administration, with no significant adverse events.ConclusionThe repeated co-administration of cilostazol and rosuvastatin in healthy male participants resulted in minor PK interactions and exhibited a safety and tolerability profile similar to those of the individual drugs. This suggested that the combined regimen is well tolerated and does not necessitate dose adjustments.RegistrationClinicalTrials.Gov identifier no. NCT06568133.
引用
收藏
页码:267 / 276
页数:10
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