CFDB - Cystic Fibrosis DataBase

ongoing trials trial from www.clinicaltrials.gov

A study to test how well BI 3720931 is tolerated and whether it improves lung function in people with cystic fibrosis (LenticlairTM 1)

Study design (if review, criteria of inclusion for studies)

Interventional - Allocation: Randomized|Intervention Model: Parallel Assignment|Masking: Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)|Primary Purpose: Treatment

Participants

Cystic Fibrosis|Bronchiectasis - 18 Years and older   (Adult, Older Adult)

Interventions

Drug: BI 1291583|Drug: Placebo

Outcome measures

Occurrence of Treatment emergent Adverse Events (TEAEs) up to 16 weeks from first drug administration|Relative change from baseline in neutrophil elastase (NE) activity in sputum at week 8 after first drug administration|Area under the concentration-time curve of the analyte in plasma over a uniform dosing interval (AUCτ) for the first dose|Maximum measured concentration of the analyte in plasma (Cmax) for the first dose|Area under the concentration-time curve of the analyte in plasma at steady state over a uniform dosing interval (AUCτ,ss)|Maximum measured concentration of the analyte in plasma (Cmax) at steady state (Cmax,ss)

Keywords: BI 129158; Clairafly; Cathepsin C Inhibitor; Anti-Inflammatory Agents - excl Steroids; pharmacological_intervention;