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Study in Adult and Adolescent Subjects With PAR (Perennial Allergic Rhinitis)

2014-08-27 03:13:16 | BioPortfolio

Summary

The purpose of the study is to assess the efficacy and safety of an investigational nasal aerosol compared with placebo nasal aerosol in the treatment of perennial allergic rhinitis.

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Investigator), Primary Purpose: Treatment

Conditions

Rhinitis, Allergic, Perennial

Intervention

Beclomethasone dipropionate hydrofluoroalkane (BDP HFA), Placebo Nasal Aerosol

Location

Teva Clinical Study Site
Los Angeles
California
United States
90025

Status

Recruiting

Source

Teva Branded Pharmaceutical Products, R&D Inc.

Results (where available)

View Results

Links

Published on BioPortfolio: 2014-08-27T03:13:16-0400

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Medical and Biotech [MESH] Definitions

Application of allergens to the nasal mucosa. Interpretation includes observation of nasal symptoms, rhinoscopy, and rhinomanometry. Nasal provocation tests are used in the diagnosis of nasal hypersensitivity, including RHINITIS, ALLERGIC, SEASONAL.

A form of non-allergic rhinitis that is characterized by nasal congestion and posterior pharyngeal drainage.

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