drugset / Trial / NCT01396278

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

NCT01396278

Phase 2 Terminated 9 enrolled Boehringer Ingelheim
RandomizedParallel-groupDouble-blindTreatment

Summary

The aim of the study is to assess and compare efficacy and safety of BI 54903 at three different dosages (b.i.d)., fluticasone propionate hydrofluoroalkane (HFA) metered dose inhaler (MDI) at a dose of 440 mcg b.i.d and low dose fluticasone propionate 88 mcg b.i.d. over an 8-week treatment period in asthmatic patients aged 12 to 65 years inadequately controlled medium dose ICS therapy as demonstrated by a decrease in forced expiratory volume in one second (FEV1) range 10 to 25 % and an asthma control questionnaire-6 (ACQ-6) equal or greater than 1.5 at time of randomisation.

Timeline

Start
2011-07-01
Primary completion
2011-12-01
Completion
2011-12-14

Drugs

EvaluationDrugModalityDoseRoute
Subject Ciclesonide Other / unclassified 90.9 ug Inhaled
Subject Ciclesonide Other / unclassified 181.8 ug Inhaled
Subject Ciclesonide Other / unclassified 363.6 ug Inhaled
Comparator Fluticasone propionate Other / unclassified 88 ug Inhaled
Comparator Fluticasone propionate Other / unclassified 440 ug Inhaled

Indications