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Ciprofloxacin Dry Powder for Inhalation (DPI) in Non-cystic Fibrosis Bronchiectasis (Non-CF BE) — RESPIRE 2  

Bronchiectasis Clinical Trial

Official title:
Randomized, Double-blind, Placebo-controlled, Multicenter Study Comparing Ciprofloxacin DPI 32.5 mg BID (Twice a Day) Intermittently Administered for 28 Days on / 28 Days Off or 14 Days on / 14 Days Off Versus Placebo to Evaluate the Time to First Pulmonary Exacerbation and Frequency of Exacerbations in Subjects With Non-Cystic Fibrosis Bronchiectasis.

Clinical Trial Summary

The purpose of this study is to evaluate if the time to first pulmonary exacerbation of bronchiectasis or its frequency can be prolonged by inhalation of ciprofloxacin for 28 days every other 28 days or for 14 days every other 14 days over 48 weeks.

Clinical Trial Description

Number of participants with Adverse events will be covered in Adverse Events section. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT02106832
Study type Interventional
Source Bayer
Contact
Status Completed
Phase Phase 3
Start date April 30, 2014
Completion date October 19, 2016
View Details
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