尼达尼布治疗特发性肺纤维化:印度视角

Anubhuti Singh, K. Kishore, A. Verma, Arpita Singh
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引用次数: 1

摘要

特发性肺纤维化(IPF)是一种与肺功能逐渐恶化并最终死亡有关的慢性疾病。直到最近,还没有药物治疗被批准用于IPF的管理,患者要么接受了症状治疗,要么参加了临床试验。自2014年以来,两种具有抗纤维化潜力的新药在大规模临床试验中取得积极成果后获得批准。宁替达尼是这类药物中最新的一种,最近在印度上市。在这里,我们对宁替达尼进行了综述,包括其作用机制、疗效、不良反应概况、成本效益和在印度环境中的影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Nintedanib for the treatment of idiopathic pulmonary fibrosis: An Indian perspective
Idiopathic pulmonary fibrosis (IPF) is a chronic disease associated with progressive deterioration of lung function and ultimately death. Until recent past, no drug therapy was approved for the management of IPF and patients either received symptomatic treatment or were enrolled in clinical trials. Since 2014, two new drugs with anti-fibrotic potential have been approved following positive outcomes in large-scale clinical trials. Nintedanib is the latest drug in this category and has recently been launched in India. Here we present a review about nintedanib, covering its mechanism of action, efficacy, adverse effect profile, cost effectiveness and implications in the Indian setting.
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