drugset / Trial / NCT00818454

4 Week 2 Way Crossover Double Blind Treatment Phase With Combivent CFC Versus Albuterol Followed by a 4 Week Open Label Combivent Respimat When All Drugs Are Used for Symptom Relief as Needed in Pts With Moderate to Severe Asthma

NCT00818454

Phase 2 Completed 226 enrolled Boehringer Ingelheim
CrossoverTreatment

Summary

The primary goal of this trial is to compare the efficacy and safety of COMBIVENT CFC MDI with albuterol HFA MDI, the current standard reliever medication in asthma. In the first cross-over part of the study (Treatment Phases 1 and 2) the marketed product, COMBIVENT CFC MDI will be used. In the second, parallel group part of the trial (Treatment Phase 3) COMBIVENT RESPIMAT will be tested for acute bronchodilator efficacy in a blinded manner at the clinic visits. During the third 4-week treatment phase open label COMBIVENT RESPIMAT will be used for symptom relief as needed.

Timeline

Start
2008-12
Primary completion
2009-09
Completion

Drugs

EvaluationDrugModalityDoseRoute
Subject Ipratropium Small molecule Inhaled
Subject Salbutamol Unknown Inhaled

Indications