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Pharmacokinetic Interaction between Rosuvastatin and Telmisartan in Healthy Korean Male Volunteers: A Randomized, Open-label, Two-period, Crossover, Multiple-dose Study

DC Field Value Language
dc.contributor.author김유경-
dc.contributor.author노혜랑-
dc.contributor.author박경수-
dc.contributor.author손미정-
dc.contributor.author손한길-
dc.contributor.author이동환-
dc.date.accessioned2015-01-06T17:15:42Z-
dc.date.available2015-01-06T17:15:42Z-
dc.date.issued2014-
dc.identifier.issn0149-2918-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/99643-
dc.description.abstractPURPOSE: Rosuvastatin, a 3-hydroxy-3-methylglutaryl-coenzyme A (HMG-CoA) reductase inhibitor, and telmisartan, an angiotensin receptor blocker, are commonly prescribed in combination for the treatment of dyslipidemia accompanied by hypertension. However, the nature of the pharmacokinetic interaction between the 2 drugs is not clearly understood. The goal of the present study was to investigate the pharmacokinetic drug-drug interaction between rosuvastatin and telmisartan in a healthy Korean population. METHODS: This was a randomized, 2-part, open-label, 2-period, crossover, multiple-dose study, with each part composed of different subjects between the ages of 20 and 55 years. In part 1, each subject received rosuvastatin 20 mg with and without telmisartan 80 mg once daily for 6 consecutive days. In part 2, each subject received telmisartan 80 mg with and without rosuvastatin 20 mg once daily for 6 consecutive days. In both parts, there was a 16-day washout period between mono- and coadministration. Blood samples were collected up to 72 hours after the last dose. Adverse events (AEs) were evaluated through interviews and physical examinations. FINDINGS: In part 1, the 90% CIs of the geometric mean ratios for the primary pharmacokinetic parameters for coadministration of the 2 drugs to monoadministration of each drug were 1.0736-1.2932 for AUCτ and 1.7442-2.3229 for Cmax,ss for rosuvastatin and 0.9942-1.1594 for AUCτ and 1.3593-1.7169 for Cmax,ss for N-desmethyl rosuvastatin, whereas in part 2, the CIs were 1.0834-1.2672 for AUCτ and 1.1534-1.5803 for Cmax,ss for telmisartan. The most frequently noted AE was cough in part 1, which occurred in 2 subjects receiving the combination therapy, and oropharyngeal pain in part 2, which occurred in 3 subjects receiving the combination therapy. All reported AEs were mild or moderate, and there was no significant difference in incidence between the treatments. IMPLICATIONS: These findings demonstrated that rosuvastatin and telmisartan mutually affected each other's pharmacokinetics, suggesting a possibility of drug-drug interaction. However, based on dose-response characteristics of the 2 drugs and previous results from other interaction studies, the degree of drug interaction observed in this study was not regarded as clinically significant. All treatments were well tolerated, with no serious AEs observed. ClinicalTrials.gov identifier: NCT01992601.-
dc.description.statementOfResponsibilityopen-
dc.format.extent1147~1158-
dc.relation.isPartOfCLINICAL THERAPEUTICS-
dc.rightsCC BY-NC-ND 2.0 KR-
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/2.0/kr/-
dc.subject.MESHAdministration, Oral-
dc.subject.MESHAdult-
dc.subject.MESHAntihypertensive Agents/administration & dosage-
dc.subject.MESHAntihypertensive Agents/adverse effects-
dc.subject.MESHAntihypertensive Agents/pharmacokinetics*-
dc.subject.MESHArea Under Curve-
dc.subject.MESHAsian Continental Ancestry Group-
dc.subject.MESHBenzimidazoles/administration & dosage-
dc.subject.MESHBenzimidazoles/adverse effects-
dc.subject.MESHBenzimidazoles/pharmacokinetics*-
dc.subject.MESHBenzoates/administration & dosage-
dc.subject.MESHBenzoates/adverse effects-
dc.subject.MESHBenzoates/pharmacokinetics*-
dc.subject.MESHCough/chemically induced-
dc.subject.MESHCross-Over Studies-
dc.subject.MESHDrug Interactions-
dc.subject.MESHDrug Therapy, Combination/adverse effects-
dc.subject.MESHHealthy Volunteers-
dc.subject.MESHHumans-
dc.subject.MESHHydroxymethylglutaryl-CoA Reductase Inhibitors/administration & dosage-
dc.subject.MESHHydroxymethylglutaryl-CoA Reductase Inhibitors/adverse effects-
dc.subject.MESHHydroxymethylglutaryl-CoA Reductase Inhibitors/pharmacokinetics*-
dc.subject.MESHMale-
dc.subject.MESHRepublic of Korea-
dc.subject.MESHRosuvastatin Calcium/administration & dosage-
dc.subject.MESHRosuvastatin Calcium/adverse effects-
dc.subject.MESHRosuvastatin Calcium/pharmacokinetics*-
dc.subject.MESHYoung Adult-
dc.titlePharmacokinetic Interaction between Rosuvastatin and Telmisartan in Healthy Korean Male Volunteers: A Randomized, Open-label, Two-period, Crossover, Multiple-dose Study-
dc.typeArticle-
dc.contributor.collegeCollege of Medicine (의과대학)-
dc.contributor.departmentDept. of Pharmacology (약리학)-
dc.contributor.googleauthorMijeong Son-
dc.contributor.googleauthorYukyung Kim-
dc.contributor.googleauthorDonghwan Lee-
dc.contributor.googleauthorHyerang Roh-
dc.contributor.googleauthorHankil Son-
dc.contributor.googleauthorJinju Guk-
dc.contributor.googleauthorSeong Bok Jang-
dc.contributor.googleauthorSu Youn Nam-
dc.contributor.googleauthorKyungsoo Park-
dc.identifier.doi10.1016/j.clinthera.2014.06.007-
dc.admin.authorfalse-
dc.admin.mappingfalse-
dc.contributor.localIdA00775-
dc.contributor.localIdA01303-
dc.contributor.localIdA01422-
dc.contributor.localIdA01968-
dc.contributor.localIdA01999-
dc.contributor.localIdA02740-
dc.relation.journalcodeJ00614-
dc.identifier.eissn1879-114X-
dc.identifier.pmid24998012-
dc.identifier.urlhttp://www.sciencedirect.com/science/article/pii/S014929181400366X-
dc.subject.keyworddrug–drug interaction-
dc.subject.keywordpharmacokinetics-
dc.subject.keywordrosuvastatin-
dc.subject.keywordtelmisartan-
dc.contributor.alternativeNameKim, Yu Kyung-
dc.contributor.alternativeNameRoh, Hye Rang-
dc.contributor.alternativeNamePark, Kyung Soo-
dc.contributor.alternativeNameSon, Mi Jeong-
dc.contributor.alternativeNameSon, Han kil-
dc.contributor.alternativeNameLee, Dong Hwan-
dc.contributor.affiliatedAuthorKim, Yu Kyung-
dc.contributor.affiliatedAuthorRoh, Hye Rang-
dc.contributor.affiliatedAuthorPark, Kyung Soo-
dc.contributor.affiliatedAuthorSon, Mi Jeong-
dc.contributor.affiliatedAuthorSon, Han kil-
dc.contributor.affiliatedAuthorLee, Dong Hwan-
dc.rights.accessRightsfree-
dc.citation.volume36-
dc.citation.number8-
dc.citation.startPage1147-
dc.citation.endPage1158-
dc.identifier.bibliographicCitationCLINICAL THERAPEUTICS, Vol.36(8) : 1147-1158, 2014-
dc.identifier.rimsid56534-
dc.type.rimsART-
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Pharmacology (약리학교실) > 1. Journal Papers

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