A Comparison of SYMBICORT® pMDI With Formoterol Turbuhaler® in Subjects With COPD

Completed · Phase 3

Conditions studied: Chronic Obstructive Pulmonary Disease

In brief

The purpose of this study is to determine if SYMBICORT® delivered via a pressurized metered-dose inhaler, referred to as a pMDI, is effective in preventing COPD exacerbations.

Key facts

Study ID
NCT00419744
Run by
AstraZeneca
People needed
1200
Starts
2007-01-01
Expected to finish
2009-08-01
Last updated by the study team
2010-09-16

Who can join

Age: 40 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

You may not qualify if…

Where it is running

Full record on ClinicalTrials.gov

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