drugset / Trial / NCT01397201

Study on BI 54903 (Inhaled Corticosteroid) Administered Twice Daily Via Respimat Inhaler in Patients With Asthma Inadequately Controlled on Low Dose Inhaled Corticosteroid (ICS)

NCT01397201

Phase 2 Terminated 30 enrolled Boehringer Ingelheim
RandomizedParallel-groupDouble-blindTreatment

Summary

The aim of the study is to assess and compare efficacy and safety of BI 54903 at 3 doses twice daily (b.i.d.), fluticasone propionate hydrofluoroalkane metered dose inhaler (HFA MDI) at a dose of 220 mcg b.i.d. and placebo b.i.d. over an 8-week treatment period in asthmatic patients aged 12 to 65 years inadequately controlled on low dose Inhaled corticosteroid (ICS) as demonstrated by a decrease in forced expiratory volume in one second (FEV1 (range 10-25%) and an asthma control questionnaire (ACQ-6) greater or equal 1.5 at time of randomisation

Timeline

Start
2011-07-01
Primary completion
2011-12-23
Completion
2011-12-23

Drugs

EvaluationDrugModalityDoseRoute
Subject Ciclesonide Other / unclassified 45.5 ug Inhaled
Subject Ciclesonide Other / unclassified 90.9 ug Inhaled
Subject Ciclesonide Other / unclassified 181.8 ug Inhaled
Comparator Fluticasone propionate Other / unclassified 220 ug Inhaled

Indications