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

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Overview

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).

Contact

For more information about this trial or to inquire about eligibility, email [email protected] or call 215-707-1359.