Pharmacokinetic Interactions Between Mirabegron and Metformin, Warfarin, Digoxin or Combined Oral Contraceptives

被引:15
|
作者
Groen-Wijnberg, Monique [1 ]
van Dijk, Jan [1 ]
Krauwinkel, Walter [1 ]
Kerbusch, Virginie [2 ]
Meijer, John [1 ]
Tretter, Reiner [1 ]
Zhang, Wenhui [3 ]
van Gelderen, Marcel [1 ]
机构
[1] Astellas Pharma Europe, Clin Pharmacol Exploratory Dev, PK&MS, Sylviusweg 62,POB 344, NL-2300 BE Leiden, Netherlands
[2] PharmAspire Consulting, Meren 1203, NL-6605 XM Wijchen, Netherlands
[3] Astellas Pharma, One Astellas Way, Northbrook, IL 60062 USA
关键词
SELECTIVE BETA(3)-ADRENOCEPTOR AGONIST; OVERACTIVE BLADDER; HEALTHY-SUBJECTS; METABOLISM;
D O I
10.1007/s13318-016-0350-5
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Background and Objectives Mirabeg ron is a selective beta 3-adrenoceptor agonist approved for the treatment of overactive bladder (OAB). Four phase 1 studies were conducted in healthy subjects to evaluate the potential for pharmacokinetic interactions between mirabegron and metformin, warfarin, digoxin, or a combination oral contraceptive (COC). Methods Thirty-two male subjects received metformin (500 mg twice daily) or mirabegron (160 mg once daily) alone, in combination or with placebo. Twenty-four male and female subjects received single doses of warfarin (25 mg) alone and in combination with mirabegron (100 mg once daily). Twenty-five male and female subjects were administered digoxin (0.25 mg) alone and in combination with mirabegron (100 mg once daily). Thirty female subjects received low-dose COC containing ethinylestradiol (EE)/levonorgestrel (LNG) (30/150 A mu g once daily) in combination with mirabegron (100 mg once daily) or placebo. Pharmacokinetic parameters were determined by non-compartmental methods. Absence of a Pharmacokinetic interaction was concluded if the 90 % confidence intervals (CI) of geometric least-squares means ratio of area under the curve (AUC) and maximum concentration (C-max) were contained within the standard 80-125 % no-effect boundaries. The effect of mirabegron on warfarin International Normalized Ratio (INR) was also assessed. Results Mirabegron increased digoxin AUC and C-max by 27 and 29 %, respectively, indicating that mirabegron is a weak inhibitor of P-glycoprotein (P-gp) in vivo. Co-administration of mirabegron did not affect the pharmacokinetics of metformin, warfarin, EE and LNG, or warfarin INR, except for a slight extension of the 90 % CI for the C-max ratio for metformin (lower limit 79 %). Metformin decreased mirabegron AUC and C-max by 21 %. Most treatment-emergent adverse events were mild, and all resolved by study end. Conclusions No dose adjustment of either drug is required when mirabegron is administered concomitantly with metformin, warfarin or COC. Patients receiving mirabegron with digoxin may require additional monitoring of digoxin concentrations with dose adjustments where necessary, due to its narrow therapeutic index.
引用
收藏
页码:417 / 429
页数:13
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