Evaluation of the Pharmacokinetic Interaction Between the β3-Adrenoceptor Agonist Mirabegron and the Muscarinic Receptor Antagonist Solifenacin in Healthy Subjects

被引:12
作者
Krauwinkel, Walter J. J. [1 ]
Kerbusch, Virginie M. M. [2 ]
Meijer, John [1 ]
Tretter, Reiner [1 ]
Strabach, Gregory [3 ]
Van Gelderen, E. Marcel [1 ]
机构
[1] Astellas Pharma Europe BV, Leiderdorp, Netherlands
[2] PharmAspire Consulting, Wijchen, Netherlands
[3] SGS, Paris, France
关键词
mirabegron; beta(3)-adrenoceptor; solifenacin; pharmacokinetic; interaction; GASTROINTESTINAL TRANSIT; METABOLISM; POTENT;
D O I
10.1002/cpdd.37
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Mirabegron, a selective beta(3)-adrenoceptor agonist, is approved for the treatment of overactive bladder (OAB). Solifenacin is a muscarinic receptor antagonist widely used in the treatment of OAB. This open-label, 1-sequence, 2-arm study investigated whether any pharmacokinetic interaction exists between mirabegron and solifenacin. In arm 1, 21 healthy men and women received 10 mg solifenacin succinate alone and in combination with mirabegron 100 mg qd. In arm 2, 20 healthy men and women received 100 mg mirabegron alone and in combination with solifenacin succinate 10mg qd. Plasma samples were collected and tolerability was assessed. Following coadministration of mirabegron and solifenacin in arm 1, solifenacin geometric mean ratios (90% confidence interval [CI]) for C-max and AUCi(nf) were 1.23 (1.15, 1.31) and 1.26 (1.17, 1.35), respectively, compared with solifenacin alone, with a 1.07-fold increase in mean t(1/2). In arm 2, mirabegron ratios (90% CI) for Cmax and AUCinf were 0.99 (0.78, 1.26) and 1.15 (1.01, 1.30), respectively, for the combination relative to mirabegron alone, with an increase in mean t(max) of approximately 1 hour. Mirabegron or solifenacin alone or in combination was generally well tolerated.
引用
收藏
页码:255 / 263
页数:9
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