drugset / Trial / NCT00476073

Efficacy and Safety of Flutiform® pMDI in Adult Patients With Mild to Moderate-severe Reversible Asthma

NCT00476073

Phase 3 Completed 228 enrolled Mundipharma Research Limited
RandomizedParallel-groupOpen-label

Summary

Open, parallel group design. The study has a screening phase and a 12 week treatment phase. Subjects will be randomised to treatment in a 1:1 ration.

Timeline

Start
2007-04
Primary completion
2008-01
Completion
2008-01

Drugs

EvaluationDrugModalityDoseRoute
Subject Fluticasone Other / unclassified 100 ug Inhaled
Subject Fluticasone Other / unclassified 250 ug Inhaled
Subject Formoterol Other / unclassified 10 ug Inhaled

Indications