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Sponsored by: |
Schering-Plough |
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Information provided by: | Schering-Plough |
ClinicalTrials.gov Identifier: | NCT00453063 |
This study is designed to assess the effectiveness of MFNS once daily compared with placebo in subjects with seasonal allergic rhinitis (SAR) in reducing the total symptom score.
Condition | Intervention | Phase |
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Seasonal Allergic Rhinitis |
Drug: Mometasone furoate nasal spray |
Phase III |
Study Type: | Interventional |
Study Design: | Treatment, Randomized, Double-Blind, Placebo Control, Parallel Assignment, Safety/Efficacy Study |
Official Title: | Placebo-Controlled Study of Mometasone Furoate Nasal Spray (MFNS) 200 Mcg QD in the Treatment of Seasonal Allergic Rhinitis |
Ages Eligible for Study: | 12 Years and older |
Genders Eligible for Study: | Both |
Accepts Healthy Volunteers: | No |
Inclusion Criteria:
Exclusion Criteria:
Study ID Numbers: | P05067 |
Study First Received: | March 26, 2007 |
Last Updated: | September 24, 2007 |
ClinicalTrials.gov Identifier: | NCT00453063 History of Changes |
Health Authority: | United States: Food and Drug Administration |
Anti-Inflammatory Agents Hypersensitivity Otorhinolaryngologic Diseases Respiratory Tract Infections Respiratory Tract Diseases Mometasone furoate |
Rhinitis, Allergic, Seasonal Hypersensitivity, Immediate Rhinitis Anti-Allergic Agents Respiratory Hypersensitivity |
Anti-Inflammatory Agents Otorhinolaryngologic Diseases Immune System Diseases Mometasone furoate Rhinitis Anti-Allergic Agents Pharmacologic Actions Nose Diseases |
Hypersensitivity Respiratory Tract Diseases Respiratory Tract Infections Rhinitis, Allergic, Seasonal Therapeutic Uses Hypersensitivity, Immediate Respiratory Hypersensitivity |