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Summary
Idiopathic pulmonary fibrosis (IPF) is a lethal lung disease with a 5‐year mortality rate of > 50% and unknown etiology. Treatment options remain limited and, currently, only two drugs are available, i.e. nintedanib and pirfenidone. However, both of these antifibrotic agents only slow down the progression of the disease, and do not remarkably prolong the survival of IPF patients. Hence,...
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