Tapinarof cream 1% once daily was well tolerated in adults and children with atopic dermatitis in two phase 3 randomized trials.

Linda Stein Gold, James Del Rosso, Benjamin D Ehst, Matthew J Zirwas, Lawrence J Green, Philip M Brown, David S Rubenstein, Stephen C Piscitelli, Anna M Tallman
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引用次数: 0

Abstract

Background: Tapinarof cream 1% once daily (QD) demonstrated significant efficacy in patients down to age 2 years with atopic dermatitis (AD) in the ADORING 1 and 2 phase 3 trials. We report local tolerability outcomes.Methods: Patients received Tapinarof or vehicle cream QD for 8 weeks. Tolerability was evaluated using patient/parent/caregiver and investigator 5-point Local Tolerability Scales (LTS). Investigators assessed tolerability for sensitive skin areas, including face/neck.Results: 813 patients were randomized (∼80% pediatric). Mean pretreatment baseline overall LTS scores were similar across groups and trials: 1.0-1.9 (patient-assessed) indicating slight burning/stinging and itching; and 0.3-0.6 (investigator-assessed) indicating no-to-minimal irritation. Tapinarof was well tolerated with improvement from pretreatment baseline and no-to-minimal burning/stinging and itching from first application through Week 8 (patient-reported): mean Week 8 LTS scores were 0.2-0.4 (burning/stinging) and 0.6-0.8 (itching). Investigators reported improvement from pretreatment baseline with no-to-minimal irritation (dryness/erythema/peeling) from first Tapinarof application through Week 8 (mean LTS scores: 0.2 and 0.1 in ADORING 1 and 2, respectively). Across sensitive skin, investigators reported no-to-minimal irritation from first application through Week 8 (mean scores [Tapinarof versus vehicle]: 0-0.3 versus 0-1.0).Conclusion: Tapinarof was well tolerated locally from first application through Week 8, including on sensitive skin areas.

Clinicaltrials.gov numbers NCT05014568, NCT05032859.

在两项3期随机试验中,每日一次1%的Tapinarof乳膏在成人和儿童特应性皮炎患者中耐受性良好。
背景:在ADORING 1期和2期3期试验中,每日一次1%的Tapinarof乳膏(QD)对2岁以下特应性皮炎(AD)患者有显著疗效。我们报告局部耐受性结果。方法:患者每日服用他匹那罗或载体乳膏8周。使用患者/家长/照顾者和研究者5点局部耐受性量表(LTS)评估耐受性。研究者评估了敏感皮肤区域的耐受性,包括面部/颈部。结果:813例患者被随机分配(约80%为儿童)。各组和试验的平均预处理基线总体LTS评分相似:1.0-1.9(患者评估)表示轻微的灼烧/刺痛和瘙痒;0.3-0.6(研究者评估)表示没有到最小的刺激。Tapinarof耐受性良好,从预处理基线开始改善,从第一次应用到第8周(患者报告),没有到最小的灼烧/刺痛和瘙痒:平均第8周LTS评分为0.2-0.4(灼烧/刺痛)和0.6-0.8(瘙痒)。研究人员报告,从第一次Tapinarof应用到第8周,从预处理基线到无到最小刺激(干燥/红斑/脱皮)的改善(ADORING 1和2的平均LTS评分分别为0.2和0.1)。在敏感皮肤上,研究人员报告,从第一次应用到第8周,没有到最小的刺激(平均评分[Tapinarof与对照品]:0-0.3对0-1.0)。结论:从首次应用到第8周,Tapinarof具有良好的局部耐受性,包括在敏感皮肤区域。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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