Ciprofloxacin (Cipro, BAYQ3939)
Drug25 mg inhaled Ciprofloxacin
NCT Number: NCT00910351
Ciprofloxacin PulmoSphere Inhalation Powder appears to be an effective and adequate antibiotic treatment for cystic fibrosis patients with P. aeruginosa colonisation. This planned study is the first study on the use of this new Ciprofloxacin PulmoSphere Inhalation Powder in the pediatric population of 6 to 12 years of age.
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Notify Me6 year–12 year
All sexes
Interventional
Phase 1
Atlanta, Georgia, United States
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
25 mg inhaled Ciprofloxacin
Time frame: Two weeks post screening
Time frame: Day 1
Bayer
Industry
A Study to Evaluate the Safety and Pharmacokinetics of Ciprofloxacin in Adults and Children Aged 6 - 12 Years With Cystic Fibrosis Following Inhalation of Ciprofloxacin Dry Powder
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