模式
药品
多元化(营销策略)
医学
药物发现
管道(软件)
药物开发
药理学
计算生物学
肿瘤科
重症监护医学
制药工业
精密医学
精确肿瘤学
医学物理学
治疗方式
数据科学
生物信息学
内科学
中国
放射肿瘤学
临床肿瘤学
梅德林
治疗方式
作者
Gui Lan Yao,Leming Shi,Yuanting Zheng
标识
DOI:10.1016/j.drudis.2025.104571
摘要
The global oncology drug pipeline is characterized by a tension between the diversification of novel targets and a persistent concentration on a few validated ones. Our analysis of 5127 drugs against 1603 targets categorizes entities as 'proven' (10.4%), 'in development' (53.6%), or 'not progressing well' (36.1%). While single-target agents dominate, dual-target strategies, driven by bispecific antibodies, are the fastest-growing approach. The top 20 proven targets attract over 50 drugs each. Small molecules remain prevalent, but novel modalities are expanding. Clinical validation of a novel target requires a median of 8.0 years with a 22.3% success rate. The USA and China drive 62.7% of global development, with the USA leading in first-in-class (FIC) innovation and China's role increasing since 2020.
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