Pharmacokinetic Interaction Between Rosuvastatin and Metformin in Healthy Korean Male Volunteers: A Randomized, Open-label, 3-period, Crossover, Multiple-dose Study

被引:11
|
作者
Lee, Donghwan [1 ,2 ]
Roh, Hyerang [1 ,2 ]
Son, Hankil [1 ,2 ]
Jang, Seong Bok [3 ]
Lee, Seoungoh [3 ]
Nam, Su Youn [3 ]
Park, Kyungsoo [1 ,2 ]
机构
[1] Yonsei Univ, Coll Med, Dept Pharmacol, Seoul 120752, South Korea
[2] Yonsei Univ, Brain Korea Plus Project Med Sci 21, Seoul 120752, South Korea
[3] Yuhan Corp, Yuhan Res Inst, Seoul, South Korea
关键词
Drug-drug interaction; metformin; pharmacokinetics; rosuvastatin; TYPE-2; DIABETES-MELLITUS; CARDIOVASCULAR COMPLICATIONS; ABCG2; POLYMORPHISM; CHINESE PATIENTS; ATORVASTATIN; EFFICACY; POPULATION; DISEASE; TRENDS; MEN;
D O I
10.1016/j.clinthera.2014.06.004
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Purpose: Rosuvastatin is indicated for hypercholesterolemia or dyslipidemia and metformin mainly for type 2 diabetes. These 2 drugs are frequently prescribed in combination due to the high comorbidity of the 2 diseases. However the nature of pharmacokinetic interaction between the 2 drugs has not been previously investigated. The purpose of our study was to investigate the pharmacokinetic interaction between rosuvastatin and metformin in healthy Korean male volunteers. Methods: This was a randomized, open-label, 6-sequence, 3-period, crossover, multiple-dose study. Eligible subjects, aged 20 to 50 years and within 20% of the ideal body weight, received 1 of the following 3 treatments for each period once daily for 5 consecutive days with a 10-day washout period between the treatments: monoadministration of rosuvastatin 10 mg tablet, monoadministration of metformin 750 mg tablet, and coadministration of rosuvastatin 10 mg tablet with metformin 750 mg tablet. Blood samples were collected up to 72 hours after the last dose and pharmacokinetic parameters for rosuvastatin and metformin were compared between combination and monotherapy. Adverse events were investigated and evaluated based on subject interviews and physical examinations. Findings: Among the 36 enrolled subjects, 31 completed the study. The coadministration of rosuvastatin with metformin produced a significant pharmacokinetic interaction in rosuvastatin C-ss,C-max, with the 90% CI for the geometric mean ratio (coadministration: monoadministration) being 110.27% to 136.39% (P = 0.0029), whereas no significant interaction was observed in rosuvastatin AUC(tau), yielding the 90% CI of 104.41% to 118.95%. When metformin was coadministered with rosuvastatin, no significant pharmacokinetic interaction was observed for C-ss,C-max and AUC(tau) of metformin, yielding the 90% CIs of the geometric mean ratio for coadministration to monoadministration as 87.38% to 102.54% and 86.70% to 99.08%, respectively. Overall, 19 mild and 1 moderate adverse events occurred in 12 subjects, with no significant differences in the incidence among the 3 treatments. Implications: Although the C-ss,C-max of rosuvastatin was significantly influenced by coadministration with metformin, the degree of interaction seen was considered clinically insignificant, with no significant interaction observed in the other pharmacokinetic measures between the 2 drugs. These results imply that drug effects of rosuvastatin and metformin will also not be significantly influenced by coadministration of the 2 drugs. All treatments were well tolerated and no serious adverse events occurred. ClinicalTrials.gov identifier: NCT01526317. (C) 2014 Elsevier HS Journals, Inc. All rights reserved.
引用
收藏
页码:1171 / 1181
页数:11
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