Novel drug targets for idiopathic pulmonary fibrosis

被引:35
|
作者
Sgalla, Giacomo [1 ]
Cocconcelli, Elisabetta [2 ]
Tonelli, Roberto [3 ]
Richeldi, Luca [1 ,4 ]
机构
[1] Southampton Univ Hosp, Southampton NIHR Resp Biomed Res Unit, Southampton, Hants, England
[2] Univ Padua, Sect Resp Dis, Dept Cardiol Thorac & Vasc Sci, Padua, Italy
[3] Univ Hosp Modena, Dept Resp Dis, Modena, Italy
[4] Southampton Univ Hosp, Fac Med, Acad Unit Clin & Expt Sci, Southampton, Hants, England
关键词
therapeutic approach; interstitial lung disease; molecular targets; nintedanib; Idiopathic pulmonary fibrosis; pirfenidone; INTERSTITIAL LUNG-DISEASE; TISSUE GROWTH-FACTOR; FORCED VITAL CAPACITY; CLINICAL-TRIAL DESIGN; SERUM AMYLOID P; AGED; 65; YEARS; N-ACETYLCYSTEINE; RANDOMIZED-TRIAL; FIBROTIC LUNG; LYSYL OXIDASE;
D O I
10.1586/17476348.2016.1152186
中图分类号
R56 [呼吸系及胸部疾病];
学科分类号
摘要
Idiopathic Pulmonary Fibrosis (IPF) is a progressive, fatal lung disorder of unknown cause with a highly variable and unpredictable clinical course. The advances made in deciphering IPF pathobiology over the last decades have led to the approval of two anti-fibrotic molecules, pirfenidone and nintedanib, that showed to be effective in significantly reducing the rate of progression of the disease. Such pharmacological breakthroughs represent a dramatic change in the management of these patients and are reflected in updated international guidelines. However, the need to find a cure for this devastating disease remains unmet and the development of novel therapeutic agents remains hurdled by several factors. Here, we review the latest insights into therapeutic approaches for IPF and the available evidence for the most promising novel compounds currently under development, and discuss the challenges and evolution of IPF clinical research over the next few years.
引用
收藏
页码:393 / 405
页数:13
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