阿普司特首次获得儿科批准

IF 3.4 3区 医学 Q1 PEDIATRICS
Hannah A Blair
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引用次数: 0

摘要

Apremilast(Otezla®)是安进公司正在开发的磷酸二酯酶-4(PDE-4)抑制剂。它已在全球多个国家(包括美国和欧盟国家)获得批准,用于治疗成人银屑病关节炎、斑块状银屑病或与白塞氏病相关的口腔溃疡。2024年4月,根据6-17岁患者的临床数据,阿普司特在美国首次获得儿科用药批准,用于治疗年龄≥6岁、体重≥20公斤、患有中重度斑块状银屑病且适合光疗或系统疗法的儿科患者。阿普司特还于2024年10月在欧盟获批用于治疗年龄≥6岁、体重≥20公斤且适合系统疗法的中重度斑块状银屑病儿童和青少年患者。本文总结了阿普司特研发过程中的里程碑,以及阿普司特首次获准用于治疗儿童斑块状银屑病的过程。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Apremilast: First Pediatric Approval.

Apremilast (Otezla®) is an inhibitor of phosphodiesterase-4 (PDE-4) being developed by Amgen. It is approved in multiple countries worldwide, including the USA and those of the EU, for the treatment of adults with psoriatic arthritis, plaque psoriasis, or oral ulcers associated with Behçet's disease. In April 2024, based on clinical data in patients aged 6-17 years, apremilast received its first pediatric approval in the USA for the treatment of pediatric patients aged ≥ 6 years and weighing ≥ 20 kg with moderate to severe plaque psoriasis who are candidates for phototherapy or systemic therapy. Apremilast was also approved in the EU in October 2024 for the treatment of moderate to severe plaque psoriasis in children and adolescents from the age of 6 years and weighing ≥ 20 kg who are candidates for systemic therapy. This article summarizes the milestones in the development of apremilast leading to the first pediatric approval for plaque psoriasis.

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来源期刊
Pediatric Drugs
Pediatric Drugs PEDIATRICS-PHARMACOLOGY & PHARMACY
CiteScore
7.20
自引率
0.00%
发文量
54
审稿时长
>12 weeks
期刊介绍: Pediatric Drugs promotes the optimization and advancement of all aspects of pharmacotherapy for healthcare professionals interested in pediatric drug therapy (including vaccines). The program of review and original research articles provides healthcare decision makers with clinically applicable knowledge on issues relevant to drug therapy in all areas of neonatology and the care of children and adolescents. The Journal includes: -overviews of contentious or emerging issues. -comprehensive narrative reviews of topics relating to the effective and safe management of drug therapy through all stages of pediatric development. -practical reviews covering optimum drug management of specific clinical situations. -systematic reviews that collate empirical evidence to answer a specific research question, using explicit, systematic methods as outlined by the PRISMA statement. -Adis Drug Reviews of the properties and place in therapy of both newer and established drugs in the pediatric population. -original research articles reporting the results of well-designed studies with a strong link to clinical practice, such as clinical pharmacodynamic and pharmacokinetic studies, clinical trials, meta-analyses, outcomes research, and pharmacoeconomic and pharmacoepidemiological studies. Additional digital features (including animated abstracts, video abstracts, slide decks, audio slides, instructional videos, infographics, podcasts and animations) can be published with articles; these are designed to increase the visibility, readership and educational value of the journal’s content. In addition, articles published in Pediatric Drugs may be accompanied by plain language summaries to assist readers who have some knowledge of, but not in-depth expertise in, the area to understand important medical advances.
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