Pfizer Inc., Groton, CT, USA.
J Clin Pharmacol. 2019 Jun;59(6):811-820. doi: 10.1002/jcph.1360. Epub 2018 Dec 17.
Atopic dermatitis is a chronic eczematous, pruritic, inflammatory skin condition affecting children and adults. Tofacitinib is a Janus kinase inhibitor. The efficacy, safety, and pharmacokinetics of 2% tofacitinib ointment twice daily have been evaluated in a 4-week phase 2a multisite randomized, double-blind, vehicle-controlled, parallel-group study (NCT02001181) in adult patients with mild to moderate atopic dermatitis and 2% to 20% body surface area (BSA) involvement. Tofacitinib ointment demonstrated significantly greater efficacy versus vehicle for all efficacy end points and had an acceptable safety profile. Predose and postdose pharmacokinetic samples were collected in week 2 and week 4. The objective of this analysis was to assess if predicted mean tofacitinib concentrations with topical application at higher treated BSA across age groups would exceed relevant concentration thresholds based on oral doses of tofacitinib. In this analysis, the pharmacokinetic concentrations were characterized using a linear mixed-effects model. The model was used to predict concentrations for adults with higher (>20%) treatable BSA. Adult concentrations were used to extrapolate concentrations to a pediatric population (2 to 17 years) using allometric principles. The predicted systemic concentrations for 2% tofacitinib ointment in both adult and pediatric populations at treated BSA ≤50% for a mild to moderate atopic dermatitis population did not exceed those reported for the 10th percentile of observed oral tofacitinib 5-mg twice-daily doses in patients with moderate to severe plaque psoriasis. The methodology described will enable analysis and prediction of systemic concentrations for topical agents.
特应性皮炎是一种慢性湿疹性、瘙痒性、炎症性皮肤病,影响儿童和成人。托法替尼是一种 Janus 激酶抑制剂。在一项为期 4 周、多中心、随机、双盲、安慰剂对照、平行组研究(NCT02001181)中,评估了每日两次外用 2%托法替尼软膏治疗轻度至中度特应性皮炎和 2%至 20%体表面积(BSA)受累的成年患者的疗效、安全性和药代动力学。托法替尼软膏在所有疗效终点均显示出明显优于安慰剂的疗效,且安全性良好。在第 2 周和第 4 周采集了给药前和给药后药代动力学样本。本分析的目的是评估在不同年龄组中,应用于较高治疗 BSA 的外用药物是否会导致预测的平均托法替尼浓度超过基于口服托法替尼剂量的相关浓度阈值。在这项分析中,使用线性混合效应模型来描述药代动力学浓度。该模型用于预测高(>20%)可治疗 BSA 的成年患者的浓度。使用体表面积比例原则,将成年患者的浓度外推至儿科人群(2 至 17 岁)。在轻度至中度特应性皮炎人群中,2%托法替尼软膏在治疗 BSA≤50%的成人和儿科人群中的预测全身浓度未超过中重度斑块型银屑病患者观察到的口服托法替尼 5mg 每日两次剂量第 10 百分位的报道。所描述的方法学将能够分析和预测外用药物的全身浓度。