药物发现
特发性肺纤维化
药物开发
医学
肺纤维化
药品
计算生物学
纤维化
药理学
生物
生物信息学
内科学
肺
作者
Simon Cruwys,Peter Hein,Bob Humphries,Darcey Black
标识
DOI:10.1016/j.drudis.2024.104207
摘要
Idiopathic pulmonary fibrosis (IPF) is an area of high unmet clinical need and high research activity in the pharmaceutical and biotech industries. The two approved therapies, nintedanib and pirfenidone, have issues with efficacy and tolerability. Despite a considerable number of development programs reaching late-stage Phase 2b or 3 clinical trials, no drug other than nintedanib and pirfenidone has successfully demonstrated a benefit for patients. An analysis of these failures, and consideration of the trajectories of some of the current development projects, may offer novel paradigms for choosing modes-of-action and for the development of successful drugs.
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