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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.
Allocation: Randomized, Control: Active Control, Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Double Blind (Subject, Caregiver, Investigator), Primary Purpose: Treatment
Albuterol DPI, Albuterol MDI, Placebo HFA MDI and Placebo DPI
Teva Clinical Study Site
Teva Branded Pharmaceutical Products, R&D Inc.
Published on BioPortfolio: 2014-08-27T03:16:16-0400
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The R-isomer of albuterol.
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Pulmonary relating to or associated with the lungs eg Asthma, chronic bronchitis, emphysema, COPD, Cystic Fibrosis, Influenza, Lung Cancer, Pneumonia, Pulmonary Arterial Hypertension, Sleep Disorders etc Follow and track Lung Cancer News ...