Gold Linda Stein, Del Rosso James, Ehst Benjamin D, Zirwas Matthew J, Green Lawrence J, Brown Philip M, Rubenstein David S, Piscitelli Stephen C, Tallman Anna M
Henry Ford Health System, Detroit, MI, USA.
JDR Dermatology Research/Thomas Dermatology, Las Vegas, NV, USA.
J Dermatolog Treat. 2025 Dec;36(1):2444489. doi: 10.1080/09546634.2024.2444489. Epub 2025 Jan 12.
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. 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. 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). Tapinarof was well tolerated locally from first application through Week 8, including on sensitive skin areas. NCT05014568, NCT05032859.
在ADORING 1和2这两项3期试验中,1%的他扎罗汀乳膏每日一次(QD)对2岁及以上的特应性皮炎(AD)患者显示出显著疗效。我们报告了局部耐受性结果。患者接受他扎罗汀或赋形剂乳膏每日一次,为期8周。使用患者/家长/护理人员和研究者的5分制局部耐受性量表(LTS)评估耐受性。研究者评估包括面部/颈部在内的敏感皮肤区域的耐受性。813名患者被随机分组(约80%为儿科患者)。各试验组的平均治疗前基线总体LTS评分相似:1.0 - 1.9(患者评估)表明有轻微灼痛/刺痛和瘙痒;0.3 - 0.6(研究者评估)表明无至轻微刺激。他扎罗汀耐受性良好,从治疗前基线有所改善,从首次应用到第8周无至轻微灼痛/刺痛和瘙痒(患者报告):第8周的平均LTS评分为0.2 - 0.4(灼痛/刺痛)和0.6 - 0.8(瘙痒)。研究者报告从治疗前基线有所改善,从首次应用他扎罗汀到第8周无至轻微刺激(干燥/红斑/脱皮)(ADORING 1和2中的平均LTS评分分别为0.2和0.1)。在整个敏感皮肤区域,研究者报告从首次应用到第8周无至轻微刺激(平均评分[他扎罗汀与赋形剂]:0 - 0.3对0 - 1.)。从首次应用到第8周,他扎罗汀在局部耐受性良好,包括在敏感皮肤区域。NCT05014568,NCT05032859。