首页> 外文期刊>The Journal of Clinical Pharmacology: Official Journal of the American College of Clinical Pharmacology >Effect of high-fat breakfast and moderate-fat evening meal on the pharmacokinetics of vardenafil, an oral phosphodiesterase-5 inhibitor for the treatment of erectile dysfunction.
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Effect of high-fat breakfast and moderate-fat evening meal on the pharmacokinetics of vardenafil, an oral phosphodiesterase-5 inhibitor for the treatment of erectile dysfunction.

机译:高脂早餐和中脂晚餐对伐地那非的药代动力学的影响,伐地那非是一种口服磷酸二酯酶5抑制剂,用于治疗勃起功能障碍。

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The effects of food on the pharmacokinetics of vardenafil were examined in 25 healthy adult males. Single-dose vardenafil 20 mg was administered in a randomized four-way crossover design after an overnight fast (at 8 a.m.), after consumption of a high-fat breakfast (at 8 a.m.), on an empty stomach (at 6 p.m.), and after a typical moderate-fat evening meal (at 6 p.m.). Serial blood samples were analyzed for vardenafil and metabolite (M1) levels. When administered after an overnight fast and after a high-fat breakfast, vardenafil geometric mean Cmax was 17.14 and 14.0 micrograms/L, respectively, and AUC was 66.78 and 67.09 micrograms./h/L, respectively; the median tmax was 1 hour under fasting conditions and 2 hours with consumption of high-fat breakfast. When administered in the evening on an empty stomach and after a moderate-fat meal, vardenafil geometric mean Cmax was 14.22 and 13.04 micrograms/L, respectively, and AUC was 51.97 and 59.12 micrograms.h/L, respectively. The median tmax was 1 hour afterfasting or a moderate-fat meal in the evening. All treatments were well tolerated. Thus, while a high-fat meal may alter Cmax slightly and delay the absorption up to 1 hour, a moderate-fat meal has no clinically relevant effect on vardenafil pharmacokinetics. Dosage changes are not warranted based on the wide therapeutic index and the efficacy observed with vardenafil in Phase III studies that were not restricted with respect to food.
机译:在25名健康成年男性中检查了食物对伐地那非药代动力学的影响。禁食过夜(上午8点),食用高脂早餐(上午8点)后,空腹(下午6点)后,以随机四次交叉设计的方式服用20剂量的伐地那非。以及典型的中脂晚餐后(下午6点)。分析了连续血样中的伐地那非和代谢物(M1)水平。隔夜禁食和高脂早餐后服用时,伐地那非的几何平均Cmax分别为17.14和14.0微克/升,AUC分别为66.78和67.09微克/小时/升;在禁食条件下,tmax中位数为1小时;在食用高脂早餐时,tmax中位数为2小时。当晚上空腹和中度胖餐后服用时,伐地那非的几何平均Cmax分别为14.22和13.04微克/升,AUC分别为51.97和59.12微克.h / L。中位tmax为禁食后1小时或晚上中度脂肪餐。所有治疗均耐受良好。因此,尽管高脂膳食可能会稍微改变Cmax并将吸收延迟至1小时,但中脂膳食对伐地那非的药代动力学没有临床相关影响。基于广泛的治疗指数和伐地那非在III期研究中观察到的疗效(不限于食品),不保证剂量改变。

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