Krauwinkel Walter, Dickinson James, Schaddelee Marloes, Meijer John, Tretter Reiner, van de Wetering Jeroen, Strabach Gregory, van Gelderen Marcel
Global Clinical Pharmacology and Exploratory Development Astellas Pharma Europe BV, R.Pharm, Sylviusweg 62, PO Box 344, 2300 AH, Leiden, The Netherlands,
Eur J Drug Metab Pharmacokinet. 2014 Mar;39(1):43-52. doi: 10.1007/s13318-013-0133-1. Epub 2013 Jun 1.
Mirabegron is a potent and selective β3-adrenoceptor agonist developed for the treatment of overactive bladder. In vitro studies demonstrated that mirabegron partly acts as a (quasi-) irreversible, metabolism-dependent inhibitor of CYP2D6. The effect of steady-state mirabegron on single doses of the sensitive CYP2D6 substrates metoprolol (100 mg) and desipramine (50 mg) was assessed in two open-label, one-sequence crossover studies in healthy subjects (CYP2D6 extensive metabolizers). Mirabegron 160 mg/day increased metoprolol maximum plasma concentration (C max) 1.90-fold (90 % confidence interval [CI] 1.54; 2.33) and total exposure (AUC0-∞) 3.29-fold (90 % CI 2.70; 4.00) in 12 males (study 1). Mean metoprolol half-life increased from 2.96 to 4.11 h. α-Hydroxymetoprolol C max and AUC to last measurable concentration decreased 2.6-fold and 2.2-fold, respectively. In study 2, mirabegron 100 mg/day increased desipramine C max 1.79-fold (90 % CI 1.69; 1.90) and AUC0-∞ 3.41-fold (90 % CI 3.07; 3.80) in 14 males and 14 females. Mean desipramine half-life increased from 19.5 to 35.8 h. C max of 2-hydroxydesipramine decreased ~twofold, while AUC increased ~1.3-fold. Desipramine was administered again 2 weeks after the last mirabegron dose. Desipramine C max and AUC0-∞ were still ~1.13-fold increased; the 90 % CIs fell within the 0.80-1.25 interval. All treatments were well tolerated. In conclusion, mirabegron is a moderate CYP2D6 inhibitor (ratio and 90 % CI <5.0).
米拉贝隆是一种强效且选择性的β3肾上腺素能受体激动剂,用于治疗膀胱过度活动症。体外研究表明,米拉贝隆部分作为一种(准)不可逆的、代谢依赖性的CYP2D6抑制剂。在两项针对健康受试者(CYP2D6广泛代谢者)的开放标签、单序列交叉研究中,评估了稳态米拉贝隆对单剂量敏感CYP2D6底物美托洛尔(100毫克)和地昔帕明(50毫克)的影响。在研究1中,12名男性服用米拉贝隆160毫克/天,美托洛尔的最大血浆浓度(Cmax)增加了1.90倍(90%置信区间[CI]为1.54;2.33),总暴露量(AUC0-∞)增加了3.29倍(90%CI为2.70;4.00)。美托洛尔的平均半衰期从2.96小时增加到4.11小时。α-羟基美托洛尔的Cmax和至最后可测量浓度的AUC分别降低了2.6倍和2.2倍。在研究2中,14名男性和14名女性服用米拉贝隆100毫克/天,地昔帕明的Cmax增加了1.79倍(90%CI为1.69;1.90),AUC0-∞增加了3.41倍(90%CI为3.07;3.80)。地昔帕明的平均半衰期从19.5小时增加到35.8小时。2-羟基地昔帕明的Cmax降低了约两倍,而AUC增加了约1.3倍。在最后一剂米拉贝隆给药2周后再次给予地昔帕明。地昔帕明的Cmax和AUC0-∞仍增加了约1.13倍;90%CI落在0.80-1.25区间内。所有治疗耐受性良好。总之,米拉贝隆是一种中度CYP2D6抑制剂(比值和90%CI<5.0)。