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
Latest Information Update: 13 Jun 2025
At a glance
- Drugs BI 1839100 (Primary)
- Indications Cough
- Focus Therapeutic Use
- Sponsors Boehringer Ingelheim
Most Recent Events
- 08 Jun 2025 Status changed from active, no longer recruiting to recruiting.
- 03 Jun 2025 Status changed from recruiting to active, no longer recruiting.
- 16 Dec 2024 Planned End Date changed from 6 Aug 2025 to 25 Mar 2026.