Clinical Trials Logo

Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00163501
Other study ID # BY9010/M1-404
Secondary ID
Status Completed
Phase Phase 3
First received September 12, 2005
Last updated November 29, 2016
Start date December 2003
Est. completion date April 2005

Study information

Verified date October 2016
Source AstraZeneca
Contact n/a
Is FDA regulated No
Health authority United States: Food and Drug Administration
Study type Interventional

Clinical Trial Summary

The purpose of this study is to investigate the safety and effectiveness of ciclesonide nasal spray as compared with placebo (inactive substance) nasal spray in relieving symptoms of perennial allergic rhinitis.


Recruitment information / eligibility

Status Completed
Enrollment 600
Est. completion date April 2005
Est. primary completion date April 2005
Accepts healthy volunteers No
Gender Both
Age group 12 Years and older
Eligibility Main Inclusion Criteria:

- General good health, other than perennial allergic rhinitis

- History and diagnosis of perennial allergic rhinitis by skin prick test

Main Exclusion Criteria:

- Participation in any investigational drug trial within the 30 days preceding the Screening Visit

- A known hypersensitivity to any corticosteroid or any of the excipients in the formulation

- Use of any prohibited concomitant medications as defined by the study protocol

Study Design

Allocation: Randomized, Intervention Model: Single Group Assignment, Masking: Double-Blind, Primary Purpose: Treatment


Intervention

Drug:
Ciclesonide


Locations

Country Name City State
United States Altana Pharma/Nycomed Atlanta Georgia
United States Altana Pharma/Nycomed Austin Texas
United States Altana Pharma/Nycomed Bethesda Maryland
United States Altana Pharma/Nycomed Cincinnati Ohio
United States Altana Pharma/Nycomed Cincinnati Ohio
United States Altana Pharma/Nycomed Clearwater Florida
United States Altana Pharma/Nycomed Cranston Rhode Island
United States Altana Pharma/Nycomed Dallas Texas
United States Altana Pharma/Nycomed Deland Florida
United States Altana Pharma/Nycomed Easton Pennsylvania
United States Altana Pharma/Nycomed Encinitas California
United States Altana Pharma/Nycomed Forked River New Jersey
United States Altana Pharma/Nycomed Houston Texas
United States Altana Pharma/Nycomed Huntington Beach California
United States Altana Pharma/Nycomed Kerrville Texas
United States Altana Pharma/Nycomed Liverpool New York
United States Altana Pharma/Nycomed Long Beach California
United States Altana Pharma/Nycomed Los Angeles California
United States Altana Pharma/Nycomed Milwaukee Wisconsin
United States Altana Pharma/Nycomed Mission Viejo California
United States Altana Pharma/Nycomed New Braunfels Texas
United States Altana Pharma/Nycomed New Orleans Louisiana
United States Altana Pharma/Nycomed Newport Beach California
United States Altana Pharma/Nycomed Normal Illinois
United States Altana Pharma/Nycomed North Dartmouth Massachusetts
United States Altana Pharma/Nycomed Oklahoma Oklahoma
United States Altana Pharma/Nycomed Overland Park Kansas
United States Altana Pharma/Nycomed Pittsburgh Pennsylvania
United States Altana Pharma/Nycomed Portland Oregon
United States Altana Pharma/Nycomed Raleigh North Carolina
United States Altana Pharma/Nycomed Richmond Virginia
United States Altana Pharma/Nycomed Salt Lake City Utah
United States Altana Pharma/Nycomed San Antonio Texas
United States Altana Pharma/Nycomed San Diego California
United States Altana Pharma/Nycomed San Diego California
United States Altana Pharma/Nycomed Skillman New Jersey
United States Altana Pharma/Nycomed Springfield New Jersey
United States Altana Pharma/Nycomed Stockton California
United States Altana Pharma/Nycomed Trumbull Connecticut
United States Altana Pharma/Nycomed Vista California
United States Altana Pharma/Nycomed Winston-Salem North Carolina

Sponsors (1)

Lead Sponsor Collaborator
AstraZeneca

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary change in Total Nasal Symptom Scores.
Secondary change in symptoms, quality of life, safety.
See also
  Status Clinical Trial Phase
Recruiting NCT05080322 - Efficacy and Safety of On-demand and Continuous Administration of Nasal Spray in the Treatment of Allergic Rhinitis Phase 4
Recruiting NCT06028490 - A Study of IL4Rα Monoclonal Antibody in Patients With Uncontrolled Seasonal Allergic Rhinitis. Phase 2
Completed NCT04388358 - Traditional Chinese Medicine for the Treatment of Perennial Allergic Rhinitis on Gut Microbiota and Immune-modulation N/A
Recruiting NCT04202263 - Assessment of Suppression of Cutaneous Allergic Responses and Pruritis by Topical Minocycline Phase 2
Completed NCT04078009 - Standardising Nasal Allergen Challenge in Adult With Hay Fever N/A
Completed NCT03644680 - Changes in Adaptive Immune Responses and Effector Cell Responses Upon Nasal Allergen Exposure - a Pilot Study N/A
Completed NCT04541004 - Adolescent Mite Allergy Safety Evaluation Phase 3
Recruiting NCT05378594 - HDM and Silver Birch NAC Standardisation N/A
Not yet recruiting NCT05684380 - Efficacy and Safety of MAZ-101 in the Treatment of Persistent Allergic Rhinitis (PER) Phase 3
Completed NCT02910401 - Clinical Response to Rhinovirus Challenge Phase 2
Completed NCT02943720 - ATIBAR - Efficacy and Safety of Two Doses of AllerT in Patients Allergic to Birch Pollen Phase 2
Not yet recruiting NCT01014325 - Safety and Efficacy Study With Allergen Extracts of House Dust Mites for Specific Sublingual Immunotherapy Phase 3
Completed NCT02556801 - Efficacy and Safety of SUBLIVAC Phleum for Immunotherapy of Grass Pollen-Allergy Phase 2
Not yet recruiting NCT02233426 - Effect of Hypertonic Solutions on Allergic Rhinitis Patients N/A
Completed NCT02352168 - Airway Inflammation in Children With Allergic Rhinitis and Intervention N/A
Completed NCT01918956 - PURETHAL Birch RUSH Study Phase 4
Completed NCT01946035 - Alpha-Blockers in Allergic Rhinitis (MAN 01) Phase 4
Completed NCT01682070 - SUBLIVAC FIX Phleum Pratense DT/DRF Phase 2
Recruiting NCT01454492 - The Relationship Between Allergic Rhinitis and Geographic Tongue N/A
Completed NCT01439815 - An Allergen BioCube (ABC) Study Evaluating the Efficacy of Fluticasone Propionate Nasal Spray Compared to Placebo Phase 4