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Lung organoids as emerging models in idiopathic pulmonary fibrosis research: Current applications, challenges, and future directions

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Therapeutic Advances in Respiratory Disease

Published online on

Abstract

Therapeutic Advances in Respiratory Disease, Volume 20, January-December 2026.
Idiopathic pulmonary fibrosis (IPF) is a devastating lung disease with progressive, irreversible scarring and a median survival of approximately 3–5 years after diagnosis. Current therapies (nintedanib, pirfenidone) modestly slow progression but do not ...