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Comparator Study Evaluating Patient Experience And Preference Of Fluticasone Furoate Nasal Spray (FFNS) Versus Fluticasone Propionate Nasal Spray (FPNS)

2014-07-24 14:20:34 | BioPortfolio

Summary

The purpose of this replicate study to FFU105924 (NCT00539006) is to provide data on subject preference of FFNS as compared with FPNS.

Description

A Randomized, Double-Blind, Placebo-Controlled, Active Comparator, One-Week, Cross-Over, Multicenter Study to Evaluate the Efficacy, Patient Preference and Experience of One-Daily, Intranasal Administration of 110mcg Fluticasone Furoate Nasal Spray (FFNS) and 200mcg Fluticasone Propionate Nasal Spray (FPNS) in Adult Subjects with Seasonal Allergic Rhinitis (FFU105927).

Each of the two treatment periods lasted one-week.

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Crossover Assignment, Masking: Double-Blind, Primary Purpose: Treatment

Conditions

Seasonal Allergic Rhinitis

Intervention

fluticasone propionate, fluticasone furoate

Location

GSK Investigational Site
Birmingham
Alabama
United States
35209

Status

Completed

Source

GlaxoSmithKline

Results (where available)

View Results

Links

Published on BioPortfolio: 2014-07-24T14:20:34-0400

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