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Sponsored by: |
Sanofi-Aventis |
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Information provided by: | Sanofi-Aventis |
ClinicalTrials.gov Identifier: | NCT00174733 |
To investigate the efficacy of ciclesonide MDI either as once daily or a twice daily regimen in patients with mild to moderate asthma, who have previously been treated with an inhaled corticosteroid.
Condition | Intervention | Phase |
---|---|---|
Asthma |
Drug: Ciclesonide |
Phase III |
Study Type: | Interventional |
Study Design: | Treatment, Randomized, Double-Blind, Placebo Control, Parallel Assignment, Efficacy Study |
Official Title: | A Multicenter, Randomized, Double-Blind, Placebo-Controlled, Parallel-Group Study to Assess the Efficacy of Ciclesonide Metered-Dose Inhaler at a Daily Dose of 160 μg Administered for Twelve Weeks Either in a Once-Daily Regimen in the Morning (160 μg qd AM) or in a Twice Daily Regimen (80 μg Bid) in Adults and Adolescents With Mild to Moderate Persistent Asthma Treated Previously With Inhaled Corticosteroids |
Ages Eligible for Study: | 12 Years and older |
Genders Eligible for Study: | Both |
Accepts Healthy Volunteers: | No |
Inclusion Criteria:
Exclusion Criteria:
Study ID Numbers: | EFC6163, XRP 1526B/3030 |
Study First Received: | September 13, 2005 |
Last Updated: | October 20, 2006 |
ClinicalTrials.gov Identifier: | NCT00174733 |
Health Authority: | United States: Food and Drug Administration |
Glucocorticosteroid. Bronchospasm |
Bronchial Spasm Ciclesonide Asthma Naphazoline Oxymetazoline Lung Diseases, Obstructive Hypersensitivity |
Respiratory Tract Diseases Guaifenesin Phenylephrine Lung Diseases Hypersensitivity, Immediate Phenylpropanolamine Respiratory Hypersensitivity |
Immune System Diseases Bronchial Diseases Therapeutic Uses Anti-Allergic Agents Pharmacologic Actions |