Suppr超能文献

用于非癌性皮肤病的生物制剂:2016年至2020年中国临床试验注册趋势分析

Biologics for Non-Cancer Dermatological Diseases: Analysis on China's Clinical Trial Registration Trend From 2016 to 2020.

作者信息

Zhu Beibei, Liu Yi, Li Jing, Ni Qi, Yin Zheng, Zhu Junli, Chen Ken, Yang Xueyuan

机构信息

Institute of Dermatology, Chinese Academy of Medical Sciences and Peking Union Medical College, Nanjing, China.

Real World Solutions, IQVIA, Shanghai, China.

出版信息

Front Pharmacol. 2022 Apr 21;13:817065. doi: 10.3389/fphar.2022.817065. eCollection 2022.

Abstract

In the past 5 years, China has quickly followed US's steps to approve the new drug application of biologics for dermatological diseases. There is an increasing interest in the current biologic landscape and further potentials in China. Our study aims to analyze features of clinical trials on non-cancer dermatological biologics and synthesize recent achievements and impediments, in order to forecast the development trends in China. Three registers (the Chinese Clinical Trial Registry, Center for Drug Evaluation, and ClinicalTrials.gov) were searched for clinical trials of non-cancer dermatological biologics initiated between 2016 and 2020 in mainland China. Trial information (the first posted year, sponsor type, study phase and site, recruitment status, disease, drug target, and drug registration type) and certain study design (selection of the control group, primary efficacy outcome, and inclusion of patient-reported outcome for non-phase I or II trials only) information were extracted and analyzed. A total of 60 trials were identified. The number of registered dermatological biologic trials significantly increased with an annual increase of 59% from 2016 to 2020, primarily driven by psoriasis (47/60, 78.3%) and atopic dermatitis (6/60, 10.0%) trials. The tumor necrosis factor (TNF)-α and interleukin (IL)-17 remained the hottest drug targets (17/60, 28.3% for TNF-α and 18/60, 30.0% for IL-17). In addition to TNF-α and IL-17, many new psoriasis drug targets came into place since 2018 (IL-12/23) and 2019 (IL-36 and glucagon-like peptide-1 (GLP-1)). Thirty percent (18/60) of the trials were conducted for biosimilar products, all of which were sponsored by local pharmaceutical companies and 88.9% of which were targeting on TNF-α. Targets of IL-36, IL-5, and IgE were only available in trials sponsored by global companies. There was great progress on the innovation of dermatological biologics in the past 5 years in China in terms of surged number of clinical trials, increased biosimilars and "me-too" drugs which greatly improved patient access to novel treatments, execution of parallel clinical trials, and improved hospital GCP office and regulatory environment. Further efforts for local pharmaceutical companies should include relocating resources to exploring novel drug targets and dermatological diseases other than psoriasis or atopic dermatitis. : [website], identifier [registration number].

摘要

在过去5年里,中国迅速效仿美国,批准了用于治疗皮肤病的生物制品新药申请。目前,中国对生物制品领域的兴趣与日俱增,且具有更大的潜力。我们的研究旨在分析非癌性皮肤病生物制品的临床试验特征,总结近期的成果与障碍,以预测中国的发展趋势。检索了三个注册库(中国临床试验注册中心、药品审评中心和美国国立医学图书馆的临床试验数据库),查找2016年至2020年期间在中国大陆启动的非癌性皮肤病生物制品的临床试验。提取并分析了试验信息(首次发布年份、申办者类型、研究阶段和地点、招募状态、疾病、药物靶点和药物注册类型)以及某些研究设计(仅针对非I期或II期试验的对照组选择、主要疗效指标以及患者报告结局的纳入情况)信息。共识别出60项试验。从2016年到2020年,注册的皮肤病生物制品试验数量显著增加,年增长率为59%,主要由银屑病(47/60,78.3%)和特应性皮炎(6/60,10.0%)试验推动。肿瘤坏死因子(TNF)-α和白细胞介素(IL)-17仍然是最热门的药物靶点(TNF-α为17/60,28.3%;IL-17为18/60,30.0%)。自2018年(IL-12/23)和2019年(IL-36和胰高血糖素样肽-1(GLP-1))以来,除了TNF-α和IL-17,许多新的银屑病药物靶点也出现了。30%(18/60)的试验是针对生物类似药产品进行的,所有这些试验均由本土制药公司申办,其中88.9%的试验针对TNF-α。IL-36、IL-

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0594/9068892/d1b3233cd16d/fphar-13-817065-g001.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验