drugset / Trial / NCT00646516

Gemini Symbicort pMDI

NCT00646516 ↗

Phase 3 Completed 615 enrolled AstraZeneca
RandomizedParallel-groupDouble-blindTreatment

Summary

The purpose of this study is to determine whether treatment with Symbicort for 12 weeks will improve lung function and symptoms of adults and adolescents with asthma.

Timeline

Start
2003-10
Primary completion
—
Completion
2005-02

Drugs

EvaluationDrugModalityDoseRoute
Subject Budesonide Small molecule 160 ug Inhaled
Subject Budesonide Small molecule 320 ug Inhaled
Subject Formoterol Other / unclassified 9 ug Inhaled

Indications