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A Dose-ranging Study to Evaluate the Safety and Efficacy of Albuterol in a Dry Powder Inhaler (DPI) and an HFA MDI

2014-08-27 03:16:16 | BioPortfolio

Summary

This study is examining how well a dry powder inhaler albuterol medication (DPI) works to help adult and adolescent subjects 12 years of age and older with persistent asthma improve lung function. During the trial the participant will also be given an HFA (hydrofluoroalkane), metered dose inhaler. albuterol. These medications will be given to the participant at two different doses. Approximately Sixty-six (66) participants will be enrolled in the study following screening and a 14 day run-in period. Participants who qualify for the study will be selected randomly to receive all of the treatments, on separate occasions, 3-7 days apart There will be 5 visits where the medications are given. The total number of clinic visit is approximately 7 visits to the clinic.

Study Design

Allocation: Randomized, Control: Active Control, Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Double Blind (Subject, Caregiver, Investigator), Primary Purpose: Treatment

Conditions

Asthma

Intervention

Albuterol DPI, Albuterol MDI, Placebo HFA MDI and Placebo DPI

Location

Teva Clinical Study Site
Huntington Beach
California
United States
92647

Status

Completed

Source

Teva Branded Pharmaceutical Products, R&D Inc.

Results (where available)

View Results

Links

Published on BioPortfolio: 2014-08-27T03:16:16-0400

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