Status:
COMPLETED
Onset of Action of Mometasone Furoate (MK-0887/SCH 032088) Nasal Spray Compared With Placebo in Seasonal Allergic Rhinitis (C93-184)
Lead Sponsor:
Organon and Co
Conditions:
Rhinitis, Allergic, Seasonal
Eligibility:
All Genders
12+ years
Phase:
PHASE3
Brief Summary
This study investigated the onset of symptom relief following initiation of treatment with mometasone furoate (MK-0887/SCH 032088) 200 mcg administered once daily compared with placebo for 14 days.
Eligibility Criteria
Inclusion
- Has a 2-year history of seasonal allergic rhinitis
- Has a positive skin test response to a local seasonal allergen (current, or performed in investigator's office within the past year)
- Is in good health and free of any unstable, clinically-significant disease, other than allergic rhinitis, that would interfere with the study schedule or evaluation of seasonal allergic rhinitis
Exclusion
- Women who are pregnant or breastfeeding
- Women of childbearing potential who are not using an acceptable form of birth control
- Has asthma that requires therapy with inhaled or systemic corticosteroids, cromolyn, or nedocromil
- Has significant renal, hepatic, neurologic, cardiovascular, hematologic, metabolic, cerebrovascular, respiratory, gastrointestinal, or other significant medical illness or disorder which, in the judgment of the investigator, could interfere with the study, or required treatment which might interfere with the study
- Is on immunotherapy with the exception of maintenance therapy
- Has a clinically significant upper respiratory or sinus infection
- Has used an investigational drug within the previous 30 days
- Has nasal structural abnormalities, including large nasal polyps and marked septal deviation, that significantly interfere with nasal air flow
- Has a history of multiple drug allergies or an allergy to antihistamines or corticoids
- Has dependence upon nasal, oral or ocular decongestants, or nasal topical antihistamines, in the opinion of the investigator
- Has rhinitis medicamentosa
- Is using of any chronic medication which could affect the course of seasonal allergic rhinitis
Key Trial Info
Start Date :
March 30 1994
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
July 7 1994
Estimated Enrollment :
201 Patients enrolled
Trial Details
Trial ID
NCT03861559
Start Date
March 30 1994
End Date
July 7 1994
Last Update
February 9 2022
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