MK0524 Seasonal Allergic Rhinitis Study
This study has been completed.
Sponsor:
Merck
Information provided by:
Merck
ClinicalTrials.gov Identifier:
NCT00533208
First received: September 19, 2007
Last updated: NA
Last verified: September 2007
History: No changes posted
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Purpose
To assess the efficacy of MK0524 on seasonal allergies.
| Condition | Intervention | Phase |
|---|---|---|
|
Seasonal Allergies |
Drug: MK0524 |
Phase 2 |
| Study Type: | Interventional |
| Study Design: | Allocation: Randomized Endpoint Classification: Safety/Efficacy Study Intervention Model: Parallel Assignment Masking: Double-Blind Primary Purpose: Treatment |
Resource links provided by NLM:
Further study details as provided by Merck:
Eligibility| Ages Eligible for Study: | 18 Years to 75 Years |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Criteria
Inclusion Criteria:
- Person has had at least 2 years of seasonal allergies
- Person has had a positive skin test to at least 1 of the allergens of the season
- Person is a non-smoker
Exclusion Criteria:
- Person has been hospitalized within the last 4 weeks
- Person is a female who has had a baby within the last 8 weeks or is still breast-feeding
Contacts and Locations
More Information
No publications provided by Merck
Additional publications automatically indexed to this study by ClinicalTrials.gov Identifier (NCT Number):
| ClinicalTrials.gov Identifier: | NCT00533208 History of Changes |
| Other Study ID Numbers: | 2007_616 |
| Study First Received: | September 19, 2007 |
| Last Updated: | September 19, 2007 |
| Health Authority: | United States: Food and Drug Administration |
Additional relevant MeSH terms:
|
Rhinitis, Allergic, Seasonal Rhinitis Nose Diseases Respiratory Tract Diseases Respiratory Hypersensitivity |
Otorhinolaryngologic Diseases Hypersensitivity, Immediate Hypersensitivity Immune System Diseases |
ClinicalTrials.gov processed this record on June 17, 2013