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10.3% 贝达齐默凝胶在日本传染性软疣患者中的安全性和耐受性。

The safety and tolerability of berdazimer gel 10.3% in Japanese patients with molluscum contagiosum.

作者信息

Kawashima Makoto, Kaneko Yoshiyuki, Sawasaki Manami, Masubuchi Kyohei, Yasukawa Hiroyuki, Okada Saki, Enloe Carolyn, Geer Carri, Cartwright Martina, Maeda-Chubachi Tomoko, Tani Takeshi

机构信息

Department of Dermatology, Tokyo Women's Medical University, Tokyo, Japan.

Sato Pharmaceutical Co., Ltd., Tokyo, Japan.

出版信息

JAAD Int. 2024 Oct 5;18:8-16. doi: 10.1016/j.jdin.2024.09.002. eCollection 2025 Feb.

Abstract

BACKGROUND

Molluscum contagiosum (MC) is a contagious viral skin infection. Berdazimer gel, 10.3% (SB206 12%) is approved in the United States as the first topical, at-home MC prescription medication.

OBJECTIVE

To assess safety and tolerability of SB206 12% in Japanese patients with MC.

METHODS

SKN15B01 (JRCT2031230123) was a phase 2, multicenter, single-group, open-label study in Japanese patients ≥2 years old with 3-70 baseline MC lesions. Patients with only periocular MC and/or immunosuppression were excluded. SB206 12% was applied once daily to lesions for 12 weeks. Safety endpoints included adverse events and local skin reactions. Exploratory efficacy endpoints included percentage of patients with complete lesion clearance and lesion count percent change from baseline.

RESULTS

Twenty patients (12 males, 8 females) with mean (range) age of 5.2 (3-13) years and mean (range) baseline lesion counts of 22.5 (8-44). Complete clearance and percent change from baseline at week 12 were 60% and -89.2%, respectively. The most common treatment-related adverse events were application site-erythema (25%,  = 5), -pain (25%,  = 5), -pruritis (25%,  = 5), and -dermatitis (20%,  = 4), all mild/moderate in severity.

LIMITATIONS

Single-group study; small sample size.

CONCLUSION

Safety and efficacy of berdazimer gel, 10.3% in Japanese patients were favorable and consistent with previous studies.

摘要

背景

传染性软疣(MC)是一种具有传染性的病毒性皮肤感染。10.3%的贝达齐默凝胶(SB206 12%)在美国被批准为首个用于家庭治疗的局部MC处方药。

目的

评估12%的SB206在日本MC患者中的安全性和耐受性。

方法

SKN15B01(JRCT2031230123)是一项2期、多中心、单组、开放标签研究,纳入年龄≥2岁、基线有3 - 70个MC皮损的日本患者。仅患有眼周MC和/或免疫抑制的患者被排除。12%的SB206每天一次涂抹于皮损处,持续12周。安全终点包括不良事件和局部皮肤反应。探索性疗效终点包括皮损完全清除的患者百分比以及与基线相比皮损计数的百分比变化。

结果

20例患者(12例男性,8例女性),平均(范围)年龄为5.2(3 - 13)岁,平均(范围)基线皮损计数为22.5(8 - 44)个。第12周时皮损完全清除率和与基线相比的百分比变化分别为60%和 - 89.2%。最常见的与治疗相关的不良事件为涂抹部位红斑(25%,n = 5)、疼痛(25%,n = 5)、瘙痒(25%,n = 5)和皮炎(20%,n = 4),均为轻度/中度。

局限性

单组研究;样本量小。

结论

10.3%的贝达齐默凝胶在日本患者中的安全性和疗效良好,与先前研究一致。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2cf4/11567095/88ce52ded869/gr1.jpg

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