drugset / Trial / NCT01058863

A Dose-ranging Study to Evaluate Albuterol and Hydrofluoroalkane in Subjects Ages 12 and Older With Persistent Asthma

NCT01058863 ↗

Phase 2 Completed 72 enrolled Teva Branded Pharmaceutical Products R&D, Inc.
RandomizedCrossoverTriple-blindTreatment

Summary

This study is examining how well a dry powder inhaler (DPI) of albuterol medication works to help adult and adolescent subjects 12 years of age and older with persistent asthma to improve lung function.

Timeline

Start
2010-02
Primary completion
2010-06
Completion
2010-06

Outcome

Met primary endpoint

registry Albuterol Spiromax® 180 mcg vs Placebo Inhaler; p <0.0001; Mean Difference (Final Values) 1.15 (95% CI 0.88 to 1.42); ANOVA NCT01058863 ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject Salbutamol Unknown 90 ug Inhaled
Subject Salbutamol Unknown 180 ug Inhaled

Indications