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
CompletedCTIS2023-510249-79-00
Boehringer Ingelheim International GmbH, Boehringer Ingelheim Espana S.A.Idiopathic pulmonary fibrosis (IPF), Progressive pulmonary fibrosis (PPF)
Start: 2024-09-10End: 2025-09-02Target: 100Updated: 2025-07-11