年龄对固定剂量克林霉素磷酸酯 1.2%/阿达帕林 0.15%/过氧化苯甲酰 3.1%凝胶治疗中重度痤疮参与者疗效和安全性的影响

L. Kircik, Julie C. Harper, Hilary Baldwin, L. Eichenfield, Emil A. Tanghetti, Emmy Graber, Heather C. Woolery-Lloyd, Z. Draelos
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引用次数: 0

摘要

简介外用克林霉素磷酸酯 1.2%/阿达帕林 0.15%/过氧化苯甲酰 3.1%(CAB)凝胶是首个获准用于治疗痤疮的固定剂量三合一配方。在对中度至重度痤疮患者进行的三项临床研究中,CAB凝胶的疗效优于载体和成分组合,而且安全性/耐受性良好。由于痤疮的发病机制和治疗效果会随着年龄的变化而变化,因此进行了这项事后分析,以评估 CAB 在儿童和青少年参与者(9-24 岁)与成人参与者(≥25 岁)中的疗效和安全性。之所以选择这一年龄分界线,是因为 18-24 岁患者的痤疮与青少年比与成人更相似,而 25 岁通常被用来定义 "成人痤疮"。研究方法在一项2期研究(NCT03170388)和两项3期研究(NCT04214652、NCT04214639)中,年龄≥9岁的中重度痤疮患者被随机分配到每日一次的CAB或载体凝胶中。终点包括获得治疗成功的参与者百分比(定义为评价者总体严重程度评分和透明/几乎透明皮肤比基线降低≥2级),以及第12周时炎症/非炎症皮损计数比基线变化的最小二乘平均百分比。此外,还评估了治疗突发不良事件(TEAE)。对所有三项研究中年龄在 9-24 岁(CAB:n=297;药物:n=218)或≥25 岁(n=91;n=51)的参与者的汇总数据进行了分析。研究结果第 12 周时,两个年龄组中约有一半接受过 CAB 治疗的参与者取得了治疗成功(9-24 岁:50.6%;≥25 岁:49.0%),而接受过药物治疗的参与者不到四分之一(两个年龄组的炎症性和非炎症性病变从基线减少了 15.7% 和 20.6%;P70%),而接受过药物治疗的参与者从基线减少了 45%-62% (P≤0.001,全部)。在这些疗效终点中,两个年龄组的 CAB 治疗参与者之间没有明显差异(P=0.68-0.97)。大多数 CAB TEAEs 的严重程度为轻度-中度,安全性/耐受性方面没有与年龄相关的趋势。结论固定剂量、三联CAB凝胶对中重度痤疮患者有效,且耐受性良好,与年龄无关。大约一半的儿童/青少年和成人患者使用CAB后皮肤变得清澈/几乎清澈,皮损数量减少>70%。资金来源:Ortho DermatologicsOrtho Dermatologics
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Impact of Age on Efficacy and Safety of Fixed-Dose Clindamycin Phosphate 1.2%/Adapalene 0.15%/Benzoyl Peroxide 3.1% Gel in Participants with Moderate-to-Severe Acne
Introduction: Topical clindamycin phosphate 1.2%/adapalene 0.15%/benzoyl peroxide 3.1% (CAB) gel is the first fixed-dose, triple-combination formulation approved for the treatment of acne. In three clinical studies of participants with moderate-to-severe acne, CAB gel demonstrated superior efficacy to vehicle and component dyads, with good safety/tolerability. As acne pathogenesis and treatment outcomes can vary with age, this post hoc analysis was performed to evaluate the efficacy and safety of CAB in pediatric and adolescent participants (aged 9-24 years) versus adult participants (≥25 years). This age cutoff was chosen as acne in patients aged 18-24 years is more similar to adolescents than adults, and age 25 is often used to define “adult acne”. Methods: In a phase 2 (NCT03170388) and two phase 3 (NCT04214652, NCT04214639) studies, participants aged ≥9 years with moderate-to-severe acne were randomized to once-daily CAB or vehicle gel. Endpoints included percentage of participants achieving treatment success (defined as ≥2-grade reduction from baseline in Evaluator’s Global Severity Score and clear/almost clear skin) and least-squares mean percent change from baseline in inflammatory/noninflammatory lesion counts at week 12. Treatment-emergent adverse events (TEAEs) were also assessed. Pooled data across all three studies were analyzed for participants aged 9-24 years (CAB: n=297; vehicle: n=218) or ≥25 years (n=91; n=51). Results: At week 12, approximately half of CAB-treated participants in both age groups achieved treatment success (9-24 years: 50.6%; ≥25: 49.0%) versus less than one-fourth with vehicle (15.7% and 20.6%; P<0.01, both). Treatment with CAB resulted in >70% reductions from baseline in inflammatory and noninflammatory lesions in both age groups, versus 45%-62% with vehicle (P≤0.001, all). There were no significant differences between CAB-treated participants in the two age groups across any of these efficacy endpoints (P=0.68-0.97). Most TEAEs with CAB were of mild-moderate severity, with no age-related trends in safety/tolerability. Conclusions: Fixed-dose, triple-combination CAB gel was efficacious and well tolerated in participants with moderate-to-severe acne, regardless of age. Approximately half of pediatric/adolescent and adult participants achieved clear/almost clear skin with CAB, and lesion count reductions of >70% were observed. Funding: Ortho Dermatologics
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