吡非尼酮
医学
特发性肺纤维化
肺活量
肺纤维化
内科学
临床试验
肺病
临床研究阶段
疾病
纤维化
临床终点
重症监护医学
胃肠病学
外科
肺
扩散能力
肺功能
作者
Talmadge E. King,Williamson Z. Bradford,Socorro Castro-Bernardini,Elizabeth A. Fagan,Ian Glaspole,Marilyn K. Glassberg,Eduard Gorina,Peter Hopkins,David Kardatzke,Lisa Lancaster,David J. Lederer,Steven D. Nathan,Carlos A. Pereira,Steven A. Sahn,Robert Sussman,Jeffrey J. Swigris,Paul W. Noble
标识
DOI:10.1056/nejmoa1402582
摘要
In two of three phase 3 trials, pirfenidone, an oral antifibrotic therapy, reduced disease progression, as measured by the decline in forced vital capacity (FVC) or vital capacity, in patients with idiopathic pulmonary fibrosis; in the third trial, this end point was not achieved. We sought to confirm the beneficial effect of pirfenidone on disease progression in such patients.
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