A Phase III, Randomised, Double-blind, Placebo-controlled Study to Assess the Efficacy, Safety, and Tolerability of BI 1291583 2.5 mg Administered Once Daily for up to 76 Weeks in Patients With Bronchiectasis (The AIRTIVITY® Study)

Status: Not yet recruiting

Phase of Trial: Phase III

Latest Information Update: 08 Apr 2025

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At a glance

Drugs BI 1291583 (Primary)
Indications Bronchiectasis
Focus Registrational; Therapeutic Use
Acronyms The AIRTIVITY Study
Sponsors Boehringer Ingelheim

Most Recent Events

18 Mar 2025 New trial record

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