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Clinical Trial Summary

This study will assess the effect of inhaled AZD5634 on Mucociliary clearance (MCC) in patients with Cystic fibrosis (CF) after single-dose administration.


Clinical Trial Description

The primary pharmacodynamic endpoint will be the average whole lung particle clearance between 0 and 60 minutes after administration of aerosolized radiolabelled particles (colloids) at Visits 2 and 3 (%MCC 0-60, whole). ;


Study Design


Related Conditions & MeSH terms


NCT number NCT02950805
Study type Interventional
Source AstraZeneca
Contact
Status Completed
Phase Phase 1
Start date May 30, 2017
Completion date April 12, 2018