Brainomix e-Lung is an FDA-cleared, CE-marked, AI-powered imaging software platform that automatically identifies and quantifies features on CT lung scans using a configured clinical workflow. Quantification of CT features can enable clinicians to more easily identify visual changes over multiple timepoints.
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Through a research collaboration and partnership with Boehringer Ingelheim, the global leader in pulmonary fibrosis therapies, Brainomix were granted privileged access to the landmark INBUILD clinical trial dataset to run the first quantitative image analysis.
The analysis used quantitative metrics from CT images. The authors were able to accurately and sensitively facilitate identification of PPF, including the assessment of PPF progression.
*This study has not been evaluated by FDA.


Results from a retrospective study with the University of Chicago, Weill Cornell Medicine, and the University of Alabama at Birmingham were presented at ERS and CHEST. The authors showed:
They could identify CT progression in 74% of patients deemed clinically stable.
They accurately identified patients at risk of developing future PPF from a single baseline scan.
*This study has not been evaluated by FDA.
“The data we have shown for e-Lung is very promising, and the ability to objectively assess parenchymal changes to predict disease trajectory and treatment responses could really help us personalize treatment decisions and improve outcomes for patients living with pulmonary fibrosis.”
A new reader study was presented at ECR 2026 by Dr Logan Sun (Royal Brompton Hospital, London). Five readers, blinded to clinical data, independently reviewed serial CTs side-by-side from 102 patients with non-IPF fibrotic ILD. All patients in this cohort demonstrated marginal FVC decline of 5 - 10%.
Readers categorized each case as either stable or progressive disease based on visually estimated changes in ILD extent.
Overlays configured to quantitatively visualize parenchymal radiological features were applied.
In cases initially categorized as stable, readers could either retain the original categorization or change to progressive. The quantitative CT imaging features were used to identify 22 to 40 cases per reader for re-evaluation. Readers changed PPF categorization in 45 - 94% of these cases, demonstrating improved reader performance.
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*This study has not been evaluated by FDA.
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