drugset / Trial / NCT06559150

A Phase II Study of Ensifentrine in Non-Cystic Fibrosis Bronchiectasis

NCT06559150

Phase 2 Recruiting 284 enrolled Verona Pharma, Inc.
RandomizedParallel-groupTriple-blindTreatment

Summary

This study is a randomized, double-blind, placebo-controlled study designed to assess the efficacy and safety of ensifentrine inhalation suspension (3 mg) delivered twice daily via standard jet nebulizer over at least 24 weeks, compared to placebo, in subjects with non-cystic fibrosis bronchiectasis (NCFBE).

Timeline

Start
2024-09-11
Primary completion
2027-09-24
Completion
2027-09-24

Drugs

EvaluationDrugModalityDoseRoute
Subject Ensifentrine Unknown 3 mg Inhaled

Indications