drugset / Trial / NCT01253473

Symbicort in Airway Predominant Chronic Obstructive Pulmonary Disease (COPD)

NCT01253473

Phase 4 Completed 46 enrolled National Jewish Health AstraZeneca · collab
RandomizedParallel-groupOpen-labelTreatment

Summary

The main objective of the study is to see if using anti-inflammatory to patients with airway disease chronic obstructive pulmonary disease (COPD) phenotype will be more effective than using these treatments in patients with loss of lung tissue. Symbicort plus ipratropium/albuterol will be used for 12 weeks in an open-label study in subjects with airway predominant COPD.

Timeline

Start
2012-04
Primary completion
2015-09
Completion
2016-01

Drugs

EvaluationDrugModalityDoseRoute
Subject Budesonide Small molecule 180 ug Inhaled
Subject budesonide/formoterol Unknown 4.5 ug Inhaled
Subject budesonide/formoterol Unknown 160 ug Inhaled
Background Ipratropium/albuterol Unknown Inhaled