An Interim Report of a Phase 3, Long-Term, Open-Label Study to Evaluate Efficacy and Safety of Difamilast Ointment in Japanese Infants with Atopic Dermatitis.

IF 3.5 3区 医学 Q1 DERMATOLOGY Dermatology and Therapy Pub Date : 2024-09-01 Epub Date: 2024-07-29 DOI:10.1007/s13555-024-01236-7
Hidehisa Saeki, Yukihiro Ohya, Naoko Baba, Tomomi Imamura, Daisuke Yokota, Hidetsugu Tsubouchi
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Abstract

Introduction: Difamilast is the first selective phosphodiesterase 4 inhibitor approved for atopic dermatitis (AD) in Japan. A phase 3, 52-week, open-label study is ongoing to establish efficacy and safety of difamilast ointments in infants with AD aged 3 to < 24 months because a clinical study has not been conducted in this population.

Methods: This study consisted of a 4-week primary evaluation period in which difamilast 0.3% ointment was applied twice daily to Japanese infants aged 3 to < 24 months (n = 41) and an ongoing 48-week long-term extension period in which difamilast 0.3% or 1% ointment was applied based on existing symptoms. The data on efficacy and safety of difamilast were obtained as of an interim report in the study period.

Results: The response rate in Investigator's Global Assessment score was 45.0% at week 1, which was maintained at 56.1% at week 4 and 63.4% at the interim report. Infants achieved the response rate in Eczema Area and Severity Index 75 (improvement of ≥ 75%) of 47.5% at week 1, which further improved to 82.9% at week 4 and 78.1% at the interim report. Adverse events (AEs) were reported in 22 (53.7%) infants in the primary evaluation period: of those the most frequent AE was nasopharyngitis (19.5%) followed by dermatitis contact (7.3%). As of the interim report, 36 (87.8%) infants experienced AEs: of those, nasopharyngitis (70.7%) and gastroenteritis (22.0%) were most frequently observed. The total AEs were mostly mild or moderate in severity. No investigational medicinal product-related AEs and no AEs leading to discontinuation were reported.

Conclusion: Difamilast ointments applied twice daily to Japanese infants with AD aged 3 to < 24 months is effective and well tolerated as of the interim report in the study period. The final results will be reported in the near future.

Clinical trial registration: Clinical Trials. gov identifier: NCT05372653.

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评估地拉米司特软膏对日本特应性皮炎婴儿疗效和安全性的 3 期长期开放标签研究中期报告
简介地拉米司特是日本首个获准用于特应性皮炎(AD)的选择性磷酸二酯酶4抑制剂。目前正在进行一项为期 52 周的开放标签 3 期研究,以确定地拉米司特软膏对 3 至 6 岁特应性皮炎婴儿的疗效和安全性:这项研究包括一个为期 4 周的初步评估期,在此期间,地拉米司特 0.3% 软膏每天两次涂抹于 3 至 3 岁的日本婴儿身上:第1周时,研究者全球评估得分的应答率为45.0%,第4周时的应答率保持在56.1%,中期报告时的应答率为63.4%。婴儿湿疹面积和严重程度指数75(改善≥75%)的应答率在第1周为47.5%,在第4周进一步提高到82.9%,在中期报告中为78.1%。在主要评估期间,22 名婴儿(53.7%)出现了不良事件(AEs):其中最常见的不良事件是鼻咽炎(19.5%),其次是接触性皮炎(7.3%)。在中期报告中,36 名婴儿(87.8%)出现了不良反应:其中最常见的是鼻咽炎(70.7%)和肠胃炎(22.0%)。所有 AE 的严重程度大多为轻度或中度。没有与研究药物相关的不良反应,也没有导致停药的不良反应:结论:地法米拉司特软膏适用于3至6岁患有AD的日本婴儿,每天两次:NCT05372653:NCT05372653。
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来源期刊
Dermatology and Therapy
Dermatology and Therapy Medicine-Dermatology
CiteScore
6.00
自引率
8.80%
发文量
187
审稿时长
6 weeks
期刊介绍: Dermatology and Therapy is an international, open access, peer-reviewed, rapid publication journal (peer review in 2 weeks, published 3–4 weeks from acceptance). The journal is dedicated to the publication of high-quality clinical (all phases), observational, real-world, and health outcomes research around the discovery, development, and use of dermatological therapies. Studies relating to diagnosis, pharmacoeconomics, public health and epidemiology, quality of life, and patient care, management, and education are also encouraged. Areas of focus include, but are not limited to all clinical aspects of dermatology, such as skin pharmacology; skin development and aging; prevention, diagnosis, and management of skin disorders and melanomas; research into dermal structures and pathology; and all areas of aesthetic dermatology, including skin maintenance, dermatological surgery, and lasers. The journal is of interest to a broad audience of pharmaceutical and healthcare professionals and publishes original research, reviews, case reports/case series, trial protocols, and short communications. Dermatology and Therapy will consider all scientifically sound research be it positive, confirmatory or negative data. Submissions are welcomed whether they relate to an International and/or a country-specific audience, something that is crucially important when researchers are trying to target more specific patient populations. This inclusive approach allows the journal to assist in the dissemination of quality research, which may be considered of insufficient interest by other journals. The journal appeals to a global audience and receives submissions from all over the world.
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