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首页> 外文期刊>Contraception >Therapeutically equivalent pharmacokinetic profile across three application sites for AG200-15, a novel low-estrogen dose contraceptive patch
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Therapeutically equivalent pharmacokinetic profile across three application sites for AG200-15, a novel low-estrogen dose contraceptive patch

机译:AG200-15(一种新型的低雌激素剂量避孕贴片)在三个应用部位的治疗等效药代动力学

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Background: AG200-15 Agile Patch (AP) is a novel 7-day contraceptive patch providing ethinyl estradiol (EE) exposure comparable to low-dose combination oral contraceptives. This study determined whether application of the AP to three different anatomical sites (lower abdomen, buttock and upper torso) influences the pharmacokinetic profile of EE and levonorgestrel (LNG). Study Design: In this open-label, three-period, crossover study, 24 subjects were randomized to one of six treatment sequences; each included application of patch to abdomen, buttock and upper torso, with the AP worn on one site for 7 days. After a 7-day washout, a new patch was applied to the next anatomical site. Multiple blood samples were collected up to 240 h after patch application. Results: For plasma EE levels, median time to maximum drug concentration (T max, 24-48 h) and mean maximum concentration (Cmax, 47.9-61.5 pg/mL) were similar among application sites. Compared with lower abdomen, EE exposure was higher (16%-30%) at buttock and upper torso (15%-22%). For plasma LNG levels, median Tmax (72-120 h) and mean C max (1436-1589 pg/mL) were similar across application sites. Compared with lower abdomen, LNG exposure was higher at buttock (1%-7%) and upper torso (16%-17%). No serious adverse events (AEs) or AE-related discontinuations occurred. The most common treatment-emergent AEs were nausea, application site pruritus and headache, with frequencies comparable across anatomical sites. Conclusions: Absorption from the abdomen was slightly lower versus other sites; however, exposure to EE and LNG for all sites was therapeutically equivalent. The AP was well tolerated at all three anatomical sites.
机译:背景:AG200-15敏捷贴剂(AP)是新型的7天避孕贴剂,与低剂量联合口服避孕药相比,可提供乙炔雌二醇(EE)暴露。这项研究确定了将AP应用于三个不同的解剖部位(小腹,臀部和上躯干)是否会影响EE和左炔诺孕酮(LNG)的药代动力学。研究设计:在这项开放性,三期,交叉研究中,将24名受试者随机分配到6个治疗序列之一。每种方法都包括在腹部,臀部和上身躯干上贴上贴剂,将AP戴在一个部位7天。冲洗7天后,将新的贴片应用于下一个解剖部位。贴剂施用后直至240小时,采集了多个血液样本。结果:对于血浆EE水平,各应用地点之间达到最大药物浓度的中位时间(T max,24-48 h)和平均最大浓度(Cmax,47.9-61.5 pg / mL)相似。与小腹相比,在臀部和上躯(15%-22%)的EE暴露较高(16%-30%)。对于血浆液化天然气水平,中位数Tmax(72-120小时)和平均Cmax(1436-1589 pg / mL)在整个应用场所相似。与小腹相比,臀部(1%-7%)和上躯干(16%-17%)的LNG暴露更高。没有发生严重的不良事件(AE)或与AE相关的停药。最常见的治疗性不良事件是恶心,应用部位瘙痒和头痛,其在各个解剖部位的发生频率相当。结论:与其他部位相比,腹部吸收稍低。但是,所有部位的EE和LNG暴露在治疗上是等效的。 AP在所有三个解剖部位均耐受良好。

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