Adis, 41 Centorian Drive, Private Bag 65901, Mairangi Bay, North Shore, 0754, Auckland, New Zealand,
Drugs Aging. 2013 Oct;30(10):853-62. doi: 10.1007/s40266-013-0112-x.
Avanafil (STENDRA™, SPEDRA™, Zepeeed™) is an oral phosphodiesterase type 5 inhibitor indicated for the treatment of erectile dysfunction. Avanafil is rapidly absorbed after oral administration, with a median time to maximum plasma concentration of 30 to 45 min. In a 12-week, randomized, double-blind, placebo-controlled, multicentre trial in patients with erectile dysfunction, avanafil 50, 100 and 200 mg recipients had significantly greater improvements from baseline than placebo recipients in mean international index of erectile dysfunction-erectile function domain scores and in successful vaginal penetration and sexual intercourse attempts (coprimary endpoints). Treatment effects were significantly larger in avanafil 100 and 200 mg recipients than 50 mg recipients. For avanafil recipients, approximately two-thirds of attempts at sexual intercourse that were made prior to 15 min, or more than 6 h, after drug administration were successful, compared with approximately one-quarter of attempts made during these time periods by placebo recipients. In trials in patients with erectile dysfunction in association with diabetes mellitus, and after nerve-sparing radical prostatectomy, avanafil 100 or 200 mg was significantly more efficacious than placebo for primary and most secondary endpoints. Avanafil was generally well tolerated in the above-mentioned studies. In a pooled analysis of three clinical trials, ≤2 % of avanafil and placebo recipients discontinued treatment because of adverse events. During extended treatment with avanafil for >52 weeks, 2.8 % of patients discontinued treatment because of adverse reactions and there were no drug-related serious adverse events.
阿伐那非(商品名:万艾可、艾力达、希爱力)是一种口服磷酸二酯酶 5 抑制剂,用于治疗勃起功能障碍。阿伐那非口服后吸收迅速,中位达峰时间为 30 至 45 分钟。在一项为期 12 周、随机、双盲、安慰剂对照、多中心的勃起功能障碍患者临床试验中,阿伐那非 50mg、100mg 和 200mg 组与安慰剂组相比,国际勃起功能指数-勃起功能域评分和阴道成功插入及性交尝试的平均改善均有显著统计学意义(主要复合终点)。阿伐那非 100mg 和 200mg 组的治疗效果明显大于 50mg 组。对于阿伐那非组,大约三分之二的性交尝试是在给药后 15 分钟之前或 6 小时之后进行的,而在这些时间范围内,安慰剂组大约四分之一的性交尝试成功。在勃起功能障碍合并糖尿病或接受保留神经的前列腺根治术后的患者临床试验中,阿伐那非 100mg 或 200mg 组在主要和大多数次要终点方面均显著优于安慰剂组。在上述研究中,阿伐那非总体上具有良好的耐受性。在三项临床试验的汇总分析中,≤2%的阿伐那非和安慰剂组因不良事件而停止治疗。在阿伐那非延长治疗超过 52 周的过程中,2.8%的患者因不良反应而停止治疗,且无药物相关的严重不良事件。