BI 1819479 for Improvement of Lung Function in Idiopathic Pulmonary Fibrosis (IPF)

A Phase 2 dose-finding study of whether the oral medicine BI 1819479 slows lung-function decline in adults 40 and older with idiopathic pulmonary fibrosis.

Phase 2Phase
CompletedStatus
NCT06335303 ↗ClinicalTrials.gov

About the study

This Phase 2 study tested three doses of BI 1819479, an investigational oral medicine, against placebo in people with idiopathic pulmonary fibrosis (IPF). The main measure was how quickly lung function (forced vital capacity) declined over up to one year. Participants could join whether or not they were taking nintedanib or pirfenidone.

Who took part

The study enrolled people who:

  • Were 40 years of age or older
  • Had idiopathic pulmonary fibrosis (IPF)
  • Were either on stable nintedanib or pirfenidone or not taking either

Status at Veritas

This study has been completed. It is no longer enrolling, and it is listed here as part of Veritas Clinical Research's track record as a research site.

Learn more

The full study record, including all eligibility criteria and outcome measures, is on ClinicalTrials.gov (NCT06335303).

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