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Therapeutic Areas: Pediatrics/Neonatology | Pulmonary/Respiratory Diseases | Family Medicine
Disease Category: Asthma (Pediatric)
Location: United States, FL
12 week dose ranging study to evaluate the efficacy and safety of Fluticasone Propionate Spiromax administered twice daily compared with placebo in adolescents and adults with persistent asthma uncontrolled on non-steroidal therapy
12 weeks study requiring 6 morning visits. Subjects should be without inhaled corticosteroids for 6 weeks prior to the screening visit.
Patient Inclustion Criteria:
Patient Exclusion Criteria:
CW ID: 180222
Date Last Changed:
July 19, 2013
Florina Shawwaf, site directorFlorida Center for Allergy and Asthma Research21150 Biscayne Blvd.
# 408Aventura, FL 33180Phone: 305-932-3252Fax: 305-933-0928
Research Center Information: Florida Center for Allergy and Asthma Research
If you would like to learn more about participating in this research study, please email the trial contact using the form below.
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