The purpose of this trial is to evaluate the effects of a single dose of denufosol versus placebo on mucociliary clearance in patients with mild to moderate CF lung disease
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Enrollment
6
Denufosol 60 mg is administered as an inhalation solution one time during the study.
Change in mucociliary clearance from baseline
Time frame: 30, 60, and 90 minutes post aerosol inhalation
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.