4.8 Review

Strategies for treating idiopathic pulmonary fibrosis

期刊

NATURE REVIEWS DRUG DISCOVERY
卷 9, 期 2, 页码 129-140

出版社

NATURE PUBLISHING GROUP
DOI: 10.1038/nrd2958

关键词

-

向作者/读者索取更多资源

Idiopathic pulmonary fibrosis (IPF) is the most common and most lethal diffuse fibrosing lung disease, with a mortality rate that exceeds that of many cancers. Recently, there have been many clinical trials of novel therapies for IPF. The results have mostly been disappointing, although two treatment approaches have shown some efficacy. This Review describes the difficulties of treating IPF and the approaches that have been tried or are in development, and concludes with suggestions of future therapeutic targets and strategies.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.8
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据