Safety of ciclesonide nasal spray administered with inhaled fluticasone dipropionate/salmeterol in adults with perennial allergic rhinitis (BY9010/M1-409)

Study identifier:BY9010/M1-409

ClinicalTrials.gov identifier:NCT00163488

EudraCT identifier:N/A

CTIS identifier:N/A

Study Complete

Official Title

Investigation of Potential Additive Inhibitory Effects on HPA-Axis of Ciclesonide Nasal Spray when Administered Concomitantly with Orally Inhaled Fluticasone Propionate/Salmeterol (FP/SAL) in Patients (18-60 Years) with Perennial Allergic Rhinitis (PAR)

Medical condition

Perennial Allergic Rhinitis

Phase

Phase 3

Healthy volunteers

No

Study drug

Ciclesonide

Sex

All

Actual Enrollment

106

Study type

Interventional

Age

18 Years - 60 Years

Date

Study Start Date: 01 Jan 2005
Primary Completion Date: 01 Aug 2005
Study Completion Date: 01 Aug 2005

Study design

Allocation: Randomized
Endpoint Classification: None
Intervention Model: Parallel Assignment
Masking: Double Blind
Primary Purpose: Treatment

Verification:

Verified 01 Oct 2016 by AstraZeneca

Sponsors

AstraZeneca

Collaborators

-

Inclusion and exclusion criteria