特发性肺纤维化
肺纤维化
药物开发
医学
离体
药物发现
重症监护医学
纤维化
专家意见
临床试验
临床前试验
药品
肺
体内
生物信息学
药理学
病理
生物
内科学
医学物理学
生物技术
作者
Toyoshi Yanagihara,Sy Giin Chong,Megan Vierhout,Jeremy A. Hirota,Kjetil Ask,Martin Kolb
标识
DOI:10.1080/17460441.2020.1755252
摘要
Based upon our current understanding, improving the identification and characterization of clinically relevant molecules or pathways responsible for progressive fibrotic diseases and use of the appropriate preclinical model system to test these will likely be required to improve the drug development pipeline for pulmonary fibrosis. Combination with appropriate preclinical models with ex vivo (precision-cut lung slices) or in vitro models would be beneficial for high-throughput drug discovery or validation of drug effects.
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