drugset / Trial / NCT00685347

Dose Response Study of Levalbuterol in the Prevention of Exercise Induced Bronchoconstriction Compared to Racemic Albuterol in Pediatric Subjects

NCT00685347

Phase 2 Completed 33 enrolled Sumitomo Pharma America, Inc.
RandomizedParallel-groupDouble-blindTreatment

Summary

The purpose of this study is to investigate, using an exercise challenge approach, the dose response of levalbuterol HFA MDI in pediatric subjects with asthma

Timeline

Start
2003-01
Primary completion
2003-06
Completion
2003-06

Drugs

EvaluationDrugModalityDoseRoute
Subject Levalbuterol Other / unclassified 45 ug
Subject Levalbuterol Other / unclassified 90 ug
Subject Levalbuterol Other / unclassified 180 ug
Comparator racemic albuterol Unknown 90 ug
Comparator racemic albuterol Unknown 180 ug
Comparator racemic albuterol Unknown 360 ug