BI 1839100 Study
A Phase IIa/IIb, randomised, double blind, placebo-controlled, parallel-group dose-finding study to examine the efficacy and safety of BI 1839100 administered orally over a 12-week treatment period in patients with idiopathic pulmonary fibrosis or progressive pulmonary fibrosis with clinically meaningful cough.
Trial Age Group: Over 18 years Over 40 years Trial Disease Type: Idiopathic Pulmonary Fibrosis (IPF) Progressive Pulmonary Fibrosis Trial Participant Type: Carer Trial Phase: Phase 2 Trial Location: ACT New Zealand NSW TAS VIC WA Trial Status: Active, not recruiting Trial Type: Interventional