메뉴 건너뛰기




Volumn 74, Issue 2, 2012, Pages 327-335

The effects of febuxostat on the pharmacokinetic parameters of rosiglitazone, a CYP2C8 substrate

Author keywords

CYP2C8; Drug drug interaction; Febuxostat; Pharmacokinetics; Rosiglitazone

Indexed keywords

CYTOCHROME P450 2C8; DRUG METABOLITE; FEBUXOSTAT; N DESMETHYLROSIGLITAZONE; PLACEBO; ROSIGLITAZONE; UNCLASSIFIED DRUG;

EID: 84863766350     PISSN: 03065251     EISSN: 13652125     Source Type: Journal    
DOI: 10.1111/j.1365-2125.2012.04182.x     Document Type: Article
Times cited : (12)

References (31)
  • 2
    • 40349110730 scopus 로고    scopus 로고
    • We can make gout management more successful now
    • Becker MA, Chohan S. We can make gout management more successful now. Curr Opin Rheumatol 2008; 20: 167-72.
    • (2008) Curr Opin Rheumatol , vol.20 , pp. 167-172
    • Becker, M.A.1    Chohan, S.2
  • 3
    • 2642527090 scopus 로고    scopus 로고
    • A retrospective study of the relationship between serum urate level and recurrent attacks of gouty arthritis: evidence for reduction of recurrent gouty arthritis with antihyperuricemic therapy
    • Shoji A, Yamanaka H, Kamatani N. A retrospective study of the relationship between serum urate level and recurrent attacks of gouty arthritis: evidence for reduction of recurrent gouty arthritis with antihyperuricemic therapy. Arthritis Rheum 2004; 51: 321-5.
    • (2004) Arthritis Rheum , vol.51 , pp. 321-325
    • Shoji, A.1    Yamanaka, H.2    Kamatani, N.3
  • 5
    • 34250724118 scopus 로고    scopus 로고
    • Lowering serum uric acid levels: what is the optimal target for improving clinical outcomes in gout?
    • Perez-Ruiz F, Liote F. Lowering serum uric acid levels: what is the optimal target for improving clinical outcomes in gout? Arthritis Rheum 2007; 57: 1324-8.
    • (2007) Arthritis Rheum , vol.57 , pp. 1324-1328
    • Perez-Ruiz, F.1    Liote, F.2
  • 7
    • 13444257733 scopus 로고    scopus 로고
    • Selectivity of febuxostat, a novel non-purine inhibitor of xanthine oxidase/xanthine dehydrogenase
    • Takano Y, Hase-Aoki K, Horiuchi H, Zhao L, Kasahara Y, Kondo S, Becker MA. Selectivity of febuxostat, a novel non-purine inhibitor of xanthine oxidase/xanthine dehydrogenase. Life Sci 2005; 76: 1835-47.
    • (2005) Life Sci , vol.76 , pp. 1835-1847
    • Takano, Y.1    Hase-Aoki, K.2    Horiuchi, H.3    Zhao, L.4    Kasahara, Y.5    Kondo, S.6    Becker, M.A.7
  • 8
    • 0037449776 scopus 로고    scopus 로고
    • An extremely potent inhibitor of xanthine oxidoreductase. Crystal structure of the enzyme-inhibitor complex and mechanism of inhibition
    • Okamoto K, Eger BT, Nishino T, Kondo S, Pai EF, Nishino T. An extremely potent inhibitor of xanthine oxidoreductase. Crystal structure of the enzyme-inhibitor complex and mechanism of inhibition. J Biol Chem 2003; 278: 1848-55.
    • (2003) J Biol Chem , vol.278 , pp. 1848-1855
    • Okamoto, K.1    Eger, B.T.2    Nishino, T.3    Kondo, S.4    Pai, E.F.5    Nishino, T.6
  • 9
    • 84863755247 scopus 로고    scopus 로고
    • Takeda Pharmaceuticals North America, Inc. Uloric® Full Prescribing Information. Deerfield, IL: Takeda Pharmaceuticals North America, Inc
    • Takeda Pharmaceuticals North America, Inc. Uloric® Full Prescribing Information. Deerfield, IL: Takeda Pharmaceuticals North America, Inc, 2011.
    • (2011)
  • 10
    • 84863756651 scopus 로고    scopus 로고
    • Takeda Canada, Inc. Uloric® Product Monograph. Mississauga, ON: Takeda Canada, Inc
    • Takeda Canada, Inc. Uloric® Product Monograph. Mississauga, ON: Takeda Canada, Inc, 2010.
    • (2010)
  • 11
    • 84863750278 scopus 로고    scopus 로고
    • Menarini International Operations. Adenuric® Product Monograph. Luxembourg Menarini International Operations Luxembourg S.A.
    • Menarini International Operations. Adenuric® Product Monograph. Luxembourg Menarini International Operations Luxembourg S.A. 2008.
    • (2008)
  • 12
    • 84863736686 scopus 로고    scopus 로고
    • Teijin Pharma Limited. Feburic® Full Prescribing Information. Chiyoda-ku, Tokyo, Japan: Teijin Pharma Limited
    • Teijin Pharma Limited. Feburic® Full Prescribing Information. Chiyoda-ku, Tokyo, Japan: Teijin Pharma Limited, 2011.
    • (2011)
  • 14
    • 14944345365 scopus 로고    scopus 로고
    • Febuxostat, a novel nonpurine selective inhibitor of xanthine oxidase: a twenty-eight-day, multicenter, phase II, randomized, double-blind, placebo-controlled, dose-response clinical trial examining safety and efficacy in patients with gout
    • Becker MA, Schumacher HR, Jr, Wortmann RL, MacDonald PA, Palo WA, Eustace D, Vernillet L, Joseph-Ridge N. Febuxostat, a novel nonpurine selective inhibitor of xanthine oxidase: a twenty-eight-day, multicenter, phase II, randomized, double-blind, placebo-controlled, dose-response clinical trial examining safety and efficacy in patients with gout. Arthritis Rheum 2005; 52: 916-23.
    • (2005) Arthritis Rheum , vol.52 , pp. 916-923
    • Becker, M.A.1    Schumacher Jr., H.R.2    Wortmann, R.L.3    MacDonald, P.A.4    Palo, W.A.5    Eustace, D.6    Vernillet, L.7    Joseph-Ridge, N.8
  • 16
    • 56049101851 scopus 로고    scopus 로고
    • Effects of febuxostat versus allopurinol and placebo in reducing serum urate in subjects with hyperuricemia and gout: a 28-week, phase III, randomized, double-blind, parallel-group trial
    • Schumacher HR, Jr, Becker MA, Wortmann RL, Macdonald PA, Hunt B, Streit J, Lademacher C, Joseph-Ridge N. Effects of febuxostat versus allopurinol and placebo in reducing serum urate in subjects with hyperuricemia and gout: a 28-week, phase III, randomized, double-blind, parallel-group trial. Arthritis Rheum 2008; 59: 1540-8.
    • (2008) Arthritis Rheum , vol.59 , pp. 1540-1548
    • Schumacher Jr., H.R.1    Becker, M.A.2    Wortmann, R.L.3    Macdonald, P.A.4    Hunt, B.5    Streit, J.6    Lademacher, C.7    Joseph-Ridge, N.8
  • 18
    • 33746865996 scopus 로고    scopus 로고
    • Pharmacokinetics, pharmacodynamics and safety of febuxostat, a non-purine selective inhibitor of xanthine oxidase, in a dose escalation study in healthy subjects
    • Khosravan R, Grabowski BA, Wu JT, Joseph-Ridge N, Vernillet L. Pharmacokinetics, pharmacodynamics and safety of febuxostat, a non-purine selective inhibitor of xanthine oxidase, in a dose escalation study in healthy subjects. Clin Pharmacokinet 2006; 45: 821-41.
    • (2006) Clin Pharmacokinet , vol.45 , pp. 821-841
    • Khosravan, R.1    Grabowski, B.A.2    Wu, J.T.3    Joseph-Ridge, N.4    Vernillet, L.5
  • 19
    • 84863736688 scopus 로고    scopus 로고
    • US Food and Drug Admisitration. Guidance for industry: drug interaction studies - study design, data analysis, and implications for dosing and labeling. US Dept of Health and Human Services, Food and Drug Administration, Center for Drug Evaluation and Research (CDER). Publication No. 6695. Available at (last accessed 16 June 2011) Rockville, MD
    • US Food and Drug Admisitration. Guidance for industry: drug interaction studies - study design, data analysis, and implications for dosing and labeling. US Dept of Health and Human Services, Food and Drug Administration, Center for Drug Evaluation and Research (CDER). Publication No. 6695. Available at (last accessed 16 June 2011) Rockville, MD, 2006.
    • (2006)
  • 20
  • 22
    • 84863750283 scopus 로고    scopus 로고
    • GlaxoSmithKline. Advandia® Prescribing Information. Research Triangle Park, NC: GlaxoSmithKline
    • GlaxoSmithKline. Advandia® Prescribing Information. Research Triangle Park, NC: GlaxoSmithKline, 2011.
    • (2011)
  • 23
    • 0033911580 scopus 로고    scopus 로고
    • Absorption, disposition, and metabolism of rosiglitazone, a potent thiazolidinedione insulin sensitizer, in humans
    • Cox PJ, Ryan DA, Hollis FJ, Harris AM, Miller AK, Vousden M, Cowley H. Absorption, disposition, and metabolism of rosiglitazone, a potent thiazolidinedione insulin sensitizer, in humans. Drug Metab Dispos 2000; 28: 772-80.
    • (2000) Drug Metab Dispos , vol.28 , pp. 772-780
    • Cox, P.J.1    Ryan, D.A.2    Hollis, F.J.3    Harris, A.M.4    Miller, A.K.5    Vousden, M.6    Cowley, H.7
  • 24
    • 0032818309 scopus 로고    scopus 로고
    • Characterization of the cytochrome P450 enzymes involved in the in vitro metabolism of rosiglitazone
    • Baldwin SJ, Clarke SE, Chenery RJ. Characterization of the cytochrome P450 enzymes involved in the in vitro metabolism of rosiglitazone. Br J Clin Pharmacol 1999; 48: 424-32.
    • (1999) Br J Clin Pharmacol , vol.48 , pp. 424-432
    • Baldwin, S.J.1    Clarke, S.E.2    Chenery, R.J.3
  • 25
    • 0036022890 scopus 로고    scopus 로고
    • The effect of ranitidine on the pharmacokinetics of rosiglitazone in healthy adult male volunteers
    • Miller AK, DiCicco RA, Freed MI. The effect of ranitidine on the pharmacokinetics of rosiglitazone in healthy adult male volunteers. Clin Ther 2002; 24: 1062-71.
    • (2002) Clin Ther , vol.24 , pp. 1062-1071
    • Miller, A.K.1    DiCicco, R.A.2    Freed, M.I.3
  • 27
    • 23044511374 scopus 로고    scopus 로고
    • Effect of quercetin on the pharmacokinetics of rosiglitazone, a CYP2C8 substrate, in healthy subjects
    • Kim KA, Park PW, Kim HK, Ha JM, Park JY. Effect of quercetin on the pharmacokinetics of rosiglitazone, a CYP2C8 substrate, in healthy subjects. J Clin Pharmacol 2005; 45: 941-6.
    • (2005) J Clin Pharmacol , vol.45 , pp. 941-946
    • Kim, K.A.1    Park, P.W.2    Kim, H.K.3    Ha, J.M.4    Park, J.Y.5
  • 28
    • 33846995662 scopus 로고    scopus 로고
    • Effect of multiple doses of montelukast on the pharmacokinetics of rosiglitazone, a CYP2C8 substrate, in humans
    • Kim KA, Park PW, Kim KR, Park JY. Effect of multiple doses of montelukast on the pharmacokinetics of rosiglitazone, a CYP2C8 substrate, in humans. Br J Clin Pharmacol 2007; 63: 339-45.
    • (2007) Br J Clin Pharmacol , vol.63 , pp. 339-345
    • Kim, K.A.1    Park, P.W.2    Kim, K.R.3    Park, J.Y.4
  • 29
    • 4544349505 scopus 로고    scopus 로고
    • Effects of trimethoprim and rifampin on the pharmacokinetics of the cytochrome P450 2C8 substrate rosiglitazone
    • Niemi M, Backman JT, Neuvonen PJ. Effects of trimethoprim and rifampin on the pharmacokinetics of the cytochrome P450 2C8 substrate rosiglitazone. Clin Pharmacol Ther 2004; 76: 239-49.
    • (2004) Clin Pharmacol Ther , vol.76 , pp. 239-249
    • Niemi, M.1    Backman, J.T.2    Neuvonen, P.J.3
  • 30
    • 19144368324 scopus 로고    scopus 로고
    • Cytochrome P450 2C8: substrates, inhibitors, pharmacogenetics, and clinical relevance
    • Totah RA, Rettie AE. Cytochrome P450 2C8: substrates, inhibitors, pharmacogenetics, and clinical relevance. Clin Pharmacol Ther 2005; 77: 341-52.
    • (2005) Clin Pharmacol Ther , vol.77 , pp. 341-352
    • Totah, R.A.1    Rettie, A.E.2
  • 31
    • 44849113881 scopus 로고    scopus 로고
    • Pharmacokinetics of oral rosiglitazone in Taiwanese and post hoc comparisons with Caucasian, Japanese, Korean, and mainland Chinese subjects
    • Chu KM, Hu OY, Pao LH, Hsiong CH. Pharmacokinetics of oral rosiglitazone in Taiwanese and post hoc comparisons with Caucasian, Japanese, Korean, and mainland Chinese subjects. J Pharm Pharm Sci 2007; 10: 411-9.
    • (2007) J Pharm Pharm Sci , vol.10 , pp. 411-419
    • Chu, K.M.1    Hu, O.Y.2    Pao, L.H.3    Hsiong, C.H.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.