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Therapeutic Areas: Pulmonary/Respiratory Diseases | Immunology | Family Medicine
Disease Category: Allergies & Asthma
Location: United States, FL

Clinical Trial Details

Overview

Research Study Summary

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

Purpose

12 weeks study requiring 6 morning visits. Subjects should be without inhaled corticosteroids for 6 weeks prior to the screening visit.

Patient Inclustion Criteria:

  • Age: > 12 years old and older
  • General good health
  • Prior asthma diagnosis
  • Current therapy: short acting bronchodilator

Patient Exclusion Criteria:

  • History of life-threatening asthma
  • Asthma exacerbations within 3 months of screening
  • History of glaucoma, cataracts, malignancy, COPD, hepatitis B or C
  • History of allergy to milk protein

To Learn more
Phase

3

Gender

Both Male and Female

Age

12 and up

Overall Status

Recruiting

Duration

12 Weeks

Facility Type

N/A

Contact

Florina Shawwaf, site director
Florida Center for Allergy and Asthma Research
21150 Biscayne Blvd.
# 408
Aventura, FL 33180
Phone: 305-932-3252
Fax: 305-933-0928

View Map

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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CW ID: 180220

Date Last Changed: July 19, 2013


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