Gordon S F
Future HealthCare Research Centers, Atlanta, GA 30340, USA.
Am J Obstet Gynecol. 1995 Sep;173(3 Pt 2):998-1004. doi: 10.1016/0002-9378(95)90250-3.
To describe the efficacy, safety, and wearability of estrogen replacement therapy of a 7-day estradiol transdermal system (Climara), developed using new drug-in-adhesive technology.
The pharmacokinetics of the 7-day system were investigated in single- and multiple-dose studies, a relative bioavailability study of the two patch sizes, and comparative studies with the twice-weekly transdermal system (Estraderm). Safety and efficacy in the treatment of vasomotor symptoms compared with conjugated equine estrogens (Premarin) and placebo were evaluated in two 11-week, randomized, double-blind, multicenter trials in 603 women; the data are combined in this report. Irritation and adhesion were also evaluated in comparative studies with Estraderm, Micropore (an inert once-weekly tape), and placebo controls.
Blood levels were sustained for the full 7 days of patch wear, there was no drug accumulation, and a physiologic estrone to estradiol ratio was maintained. Pharmacokinetics studies showed dose proportionality of the 0.05 and 0.1 mg/day patches. Both patch sizes significantly decreased the frequency of hot flushes compared with placebo and were comparable with conjugated equine estrogens. There was a statistically significant difference between the two patch sizes. The mean overall decline in the hot flush rate was 74.6% for the 0.1 mg patch versus 64.5% for the 0.05 mg patch (p < or = 0.05). The combined data also showed that the onset of efficacy is within 1 to 2 weeks after the start of therapy and that efficacy is fully sustained during the 7-day patch wear period with some diminution of effect during the treatment-free week of each cycle. Treatment was well tolerated. Adverse events led to withdrawal from the studies in 8.9% of subjects. In most of these (6.8% of subjects), the cause was adverse skin reactions. Skin irritation was similar to Estraderm in comparative studies, whereas adhesion was significantly better with Climara.
The Climara patch delivers estradiol for a full 7 days. Clinical efficacy of both patch sizes is comparable with currently accepted therapy and is sustained for the entire week of patch wear. A significant difference in response between the two doses supports dose titration. The patch is well tolerated and has excellent adhesion.
描述采用新型药物黏附技术研发的7天雌二醇透皮系统(克龄蒙)进行雌激素替代疗法的疗效、安全性和可佩戴性。
在单剂量和多剂量研究、两种贴片尺寸的相对生物利用度研究以及与每周两次透皮系统(爱斯妥)的对比研究中,对7天系统的药代动力学进行了研究。在两项针对603名女性的为期11周的随机、双盲、多中心试验中,评估了与结合马雌激素(倍美力)和安慰剂相比,其在治疗血管舒缩症状方面的安全性和疗效;本报告中合并了这些数据。还在与爱斯妥、微孔胶带(一种惰性的每周一次胶带)和安慰剂对照的对比研究中评估了刺激性和黏附性。
贴片佩戴的整整7天内血药水平持续稳定,无药物蓄积,且维持了生理上的雌酮与雌二醇比例。药代动力学研究表明,0.05毫克/天和0.1毫克/天的贴片具有剂量比例性。与安慰剂相比,两种贴片尺寸均显著降低了潮热频率,且与结合马雌激素相当。两种贴片尺寸之间存在统计学显著差异。0.1毫克贴片的潮热率平均总体下降74.6%,而0.05毫克贴片为64.5%(p≤0.05)。综合数据还显示,疗效在治疗开始后1至2周内出现,且在7天贴片佩戴期内疗效完全维持,每个周期的无治疗周期间效果略有减弱。治疗耐受性良好。不良事件导致8.9%的受试者退出研究。在大多数此类情况(6.8%的受试者)中,原因是皮肤不良反应。在对比研究中,皮肤刺激性与爱斯妥相似,而克龄蒙的黏附性明显更好。
克龄蒙贴片可提供整整7天的雌二醇。两种贴片尺寸的临床疗效与目前公认的疗法相当,且在贴片佩戴的整个星期内持续有效。两种剂量之间的反应存在显著差异,支持剂量滴定。该贴片耐受性良好,黏附性极佳。