Mometasone Furoate Aqueous (MK-0887/SCH 032088) Nasal Spray vs Placebo and FLONASE® in Seasonal Allergic Rhinitis Patients (I94-001)

Phase 3CompletedNCT03882047

Organon and Co313 enrolled

Overview

The purpose of this study is to evaluate the efficacy and safety of mometasone furoate (SCH 32088) aqueous nasal spray 200 mcg once daily compared to placebo once daily in the treatment of participants with seasonal allergic rhinitis. Flonase (fluticasone propionate) nasal spray 200 mcg once daily has been chosen as the active control for this study.

Study Type

INTERVENTIONAL

Allocation

RANDOMIZED

Purpose

TREATMENT

Masking

DOUBLE

Enrollment

313

Conditions

Rhinitis, Allergic, Seasonal

Interventions

Mometasone furoateDRUG

Mometasone furoate nasal spray, 200 mg once daily

Fluticasone propionateDRUG

Fluticasone propionate nasal spray, 200 mg once daily

Mometasone furoate placeboDRUG

Mometasone furoate placebo matching nasal spray, once daily

Eligibility

Sex: ALLMin age: 12 Years

Medical Language ↔ Plain English

Inclusion Criteria: * 2-year history of seasonal allergic rhinitis * Positive skin test response to a local seasonal allergen (current, or performed in investigator's office within the past year) * 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 Criteria: * Women who are pregnant or breastfeeding * Women of childbearing potential who are not using an acceptable form of birth control * Significant history of metabolic, cardiovascular, neurologic, hematologic, hepatic, gastrointestinal, cerebrovascular, respiratory, or renal disease, or any other disorder which, in the judgment of the investigator, could interfere with the study, or require treatment which might interfere with the study * Use of any chronic medication which could affect the course of seasonal allergic rhinitis * Asthma requiring chronic use of inhaled or systemic corticosteroids (inhaled bronchodilators are permitted for asthma treatment) * Current or history of frequent, clinically significant sinusitis or chronic purulent postnasal drip * Upper respiratory tract or sinus infection that requires antibiotic therapy within the previous 2 weeks, or a viral upper respiratory infection (URI) within the 7 days prior to Screening * Dependence upon nasal, oral or ocular decongestants, or nasal topical antihistamines, in the opinion of the investigator * Has rhinitis medicamentosa * Investigational drug use within the previous 30 days * Nasal structural abnormalities, including large nasal polyps and marked septal deviation, that significantly interfere with nasal air flow * Immunotherapy (desensitization therapy), unless on a stable maintenance schedule for at least one month prior to the Screening visit * History of multiple drug allergies, allergy to antihistamines or corticoids * History of psychosis, antagonistic personality, poor motivation, hypochondriasis, or any other emotional or intellectual problems that are likely to limit the validity of consent to participate in the study

Outcomes

Primary Outcomes

Change From Baseline in Total Nasal Symptom Score Averaged Over Day 1 Through Day 15 (Based on Participant Diaries)

Change from baseline averaged over study Day 1 through study Day 15 was calculated for Total Nasal Symptom Score, based on participant diaries. Participants scored 4 symptoms (rhinorrhea, stuffiness, itching, sneezing) in their diaries using the following scale: 0=none, 1=mild, 2=moderate, 3=severe. The Total Nasal Symptom Score was the sum of the 4 individual scores (range=0-12; higher score indicating more frequent/severe nasal symptoms.) Change from baseline was the 15-day average score minus the baseline score. Scores were recorded twice daily, in the morning (AM) and night (PM). Average AM/PM scores were first calculated separately, then averaged together to obtain the 15-day average score. Baseline score was an average of the 3 AM scores and 3 PM scores preceding treatment. Negative changes indicated a decrease in symptom severity.

Time frame: Baseline and Day 1 through Day 15 (averaged over 15 days)

Secondary Outcomes

Change From Baseline in the Total Nasal Symptom Score at Day 4 (Physician Evaluation)

Change from baseline at Day 4 was calculated for the Total Nasal Symptom Score, as assessed by the physician. The Total Nasal Symptom Score was a composite of the following symptoms: rhinorrhea, nasal stuffiness, nasal itching, and sneezing scores. The physician scored each symptom during the study visit on the following scale: 0=none, 1=mild, 2=moderate; and 3=severe. The composite score ranged from 0-12. Change from baseline = visit score - baseline score (Day 1 visit). A negative change from baseline score indicated a decrease in symptom severity.

Time frame: Baseline (Day 1) and Day 4

Change From Baseline in the Total Nasal Symptom Score at Day 15 (Physician Evaluation)

Change from baseline at Day 15 was calculated for the Total Nasal Symptom Score, as assessed by the physician. The Total Nasal Symptom Score was a composite of the following symptoms: rhinorrhea, nasal stuffiness, nasal itching, and sneezing scores. The physician scored each symptom during the study visit on the following scale: 0=none, 1=mild, 2=moderate; and 3=severe. The composite score ranged from 0-12. Change from baseline = visit score - baseline score (Day 1 visit). A negative change from baseline score indicated a decrease in symptom severity.

Data from ClinicalTrials.gov

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