Kim Dong Ho, Hong Jang Hee, Jung Won Tae, Nam Kyu-Yeol, Roh Jae Seok, Lee Hye Jung, Moon JungHa, Kim Kyu Yeon, Jung Jin-Gyu, Sunwoo Jung
Clinical Trials Center, Chungnam National University Hospital, 266 Munhwa-ro, Jung-gu, Daejeon, Republic of Korea.
Department of Medical Science, Chungnam National University College of Medicine, Daejeon, Republic of Korea.
Am J Cardiovasc Drugs. 2025 Mar;25(2):267-276. doi: 10.1007/s40256-024-00686-w. Epub 2024 Nov 2.
Cilostazol 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.
A 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.
Fifty-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 (C) and area under the plasma concentration-time curve during the dosing interval at steady state (AUC) indicated no significant interaction between cilostazol and rosuvastatin. Safety assessments showed comparable profiles to individual drug administration, with no significant adverse events.
The 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.
ClinicalTrials.Gov identifier no. NCT06568133.
西洛他唑可改善缺血症状并预防脑梗死复发,瑞舒伐他汀可降低胆固醇水平。然而,尚无关于这两种药物在健康成年人中的药代动力学相互作用的报道。本研究评估了西洛他唑和瑞舒伐他汀联合应用于健康男性受试者时的药代动力学(PK)相互作用及安全性。
进行了一项随机、开放标签、多剂量、双臂、两阶段研究。A组有30名受试者,每天接受200毫克西洛他唑,B组有27名受试者,每天接受20毫克瑞舒伐他汀,持续7天。在第二阶段,经过7天的洗脱期后,两组受试者每天联合接受200毫克西洛他唑和20毫克瑞舒伐他汀,持续7天。使用液相色谱-串联质谱法定量测定西洛他唑及其代谢产物和瑞舒伐他汀的血浆浓度。
57名受试者被随机分组,44名完成了研究。稳态时最大血浆浓度(C)和稳态给药间隔期间血浆浓度-时间曲线下面积(AUC)的几何平均比值(GMR)和90%置信区间(CI)表明西洛他唑和瑞舒伐他汀之间无显著相互作用。安全性评估显示与单独用药的情况相当,无显著不良事件。
在健康男性受试者中重复联合使用西洛他唑和瑞舒伐他汀导致轻微的PK相互作用,且安全性和耐受性与单独用药相似。这表明联合用药方案耐受性良好,无需调整剂量。
ClinicalTrials.Gov标识符:NCT06568133