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Idiopathic pulmonary fibrosis (IPF) is a fibrosing interstitial lung disease (ILD) of unknown aetiology with a median survival of only 2–5 years. It is characterized by progressive dyspnoea and worsening lung function, ultimately resulting in death.
Until recently, there were no effective therapies for IPF; however, with the publication of two landmark clinical trials in 2014, the anti‐fibrotic therapies,...
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