IPF diagnosis relies on clinical evaluation, HRCT, and occasionally lung biopsy to identify usual interstitial pneumonia patterns. The average time to IPF diagnosis can be delayed up to two years ...

"As we put together imaging of patients, a lot of them over three, six, nine months or more had CT scans that showed ... from patients who had idiopathic pulmonary fibrosis, or IPF.

IPF severely impacts quality of life, limiting daily activities due to progressive respiratory decline. Median survival for IPF patients is approximately 3 to 5 years post-diagnosis. The financial ...