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Updated: May 17, 2026

Unilateral Lung Volume Analysis Using Micro-CT for Enhanced Assessment of Pulmonary Fibrosis in Preclinical Models
Published on: June 20, 2025
Current and novel drug therapies for idiopathic pulmonary fibrosis
Huzaifa I Adamali1, Toby M Maher
1Interstitial Lung Disease Unit, Royal Brompton Hospital, London, UK.
Abstract:
Over the past decade, there has been a cohesive effort from patients, physicians, clinical and basic scientists, and the pharmaceutical industry to find definitive treatments for idiopathic pulmonary fibrosis (IPF). As understanding of disease behavior and pathogenesis has improved, the aims of those treating IPF have shifted from reversing the disease to slowing or preventing progression of this chronic fibrotic illness. It is to be hoped that by slowing disease progression, survival will be improved from the current dismal median of 3.5 years following diagnosis. In Europe and Asia, a milestone has recently been reached with the licensing of the first IPF-specific drug, pirfenidone. This review assesses the current treatment modalities available for IPF, including pirfenidone. It also turns an eye to the future and discusses the growing number of promising compounds currently in development that it is hoped, in time, will make their way into the clinic as treatments for IPF.
Insights
Researchers are exploring new treatments for idiopathic pulmonary fibrosis (IPF). The focus is on slowing disease progression to improve patient survival, with pirfenidone now available and more drugs in development.
Area of Science:
- Pulmonary Medicine
- Pharmacology
Background:
- Idiopathic pulmonary fibrosis (IPF) is a chronic, progressive fibrotic lung disease with limited treatment options.
- Current therapeutic strategies aim to slow disease progression rather than reverse it, given the poor median survival rate of 3.5 years.
Purpose of the Study:
- To review current treatment modalities for IPF.
- To discuss emerging therapeutic compounds in the pipeline for IPF treatment.
Main Methods:
- Literature review of existing IPF treatments.
- Analysis of ongoing research and development for novel IPF therapies.
Main Results:
- Pirfenidone, the first IPF-specific drug, has been licensed in Europe and Asia.
- Numerous promising compounds are under investigation for future clinical application.
Conclusions:
- The treatment landscape for IPF is evolving, with a shift towards disease-modifying therapies.
- Future treatments hold promise for improving outcomes in patients with IPF.
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