An Exploratory Study of Nasonex in Patients With Moderate to Severe Persistent Allergic Rhinitis and Intermittent Asthma
Status and phase
Conditions
Treatments
Details and patient eligibility
About
The primary objective of this study is to explore the efficacy of Nasonex (mometasone furoate nasal spray) in comparison with placebo in improving the quality of life of subjects with moderate to severe persistent allergic rhinitis and intermittent asthma. A secondary objective is to evaluate the efficacy of Nasonex in relieving the subject's symptoms of allergic rhinitis and asthma.
Full description
The primary objective is to explore the efficacy of mometasone furoate nasal spray (MFNS) in comparison with placebo in improving the quality of life of subjects with moderate to severe persistent allergic rhinitis and intermittent asthma as measured by the Rhinasthma Questionnaire (Global Summary Score). In addition, there are two secondary objectives. The first secondary objective is to evaluate the efficacy of MFNS in improving the quality of life of subjects with moderate to severe persistent allergic rhinitis and intermittent asthma as measured by the Rhinasthma Upper Airways Score, the Rhinasthma Lower Airways Score, and the Rhinasthma Respiratory Allergy Impact Score. The second secondary objective is to evaluate the efficacy of MFNS in relieving the subject's symptoms of allergic rhinitis and asthma as measured by the Total 5 Symptoms Score (T5SS) and the Global Symptom Score (T5SS+asthma symptoms) and by the use of rescue medication on demand.
Enrollment
Sex
Ages
Volunteers
Inclusion criteria
- Outpatients (≥18 and ≤ 75 years of age) of either sex
- Willingness to participate and comply with procedures by signing a written informed consent
- Moderate/severe persistent allergic rhinitis with a history of intermittent asthma from at least 2 years and actual asthma (symptoms in the last 4 weeks)
- To qualify at the randomization visit the daily average of the T5SS [(Morning-time T5SS + Evening-time T5SS)/2] had to be ≥ 6 in at least 4 days during the 1 week run-in period
- Positive (weal diameter >3 mm) skin prick test (SPT) and/or CAP-RAST (class II or higher) performed in the 6 months prior to the start of the trial were required for at least house dust mite and 1 pollen allergen (grass or Parietaria, IgE level >3.5 U/mL)
- All prior medication washout times had been observed
- Female volunteers of childbearing potential had to agree to use a medically accepted method of contraception or be surgically sterilized prior to screening, while receiving protocol-specified medication, and for 30 days after stopping the medication
- Negative urine pregnancy test
- Free of any clinically relevant disease that would have interfered with study evaluations
- Able to adhere to the dosing and visit schedules, and agree to record symptom severity scores and use of IMP and rescue medications in a daily diary
Exclusion criteria
- Female who was or intended to become pregnant during the study or within 12 weeks after study completion
- Nursing, or intended to be nursing during the study or within 12 months after study completion
- Taking medications prohibited during the study or had not complied with the requirements for the designated washout periods for any of the prohibited medications
- Anatomical abnormalities of the nose (turbinate hypertrophy, septal deviation, polyps)
- Acute or chronic sinusitis currently being treated with antibiotics and/or topical or oral decongestants
- Rhinitis medicamentosa
- Evidence of persistent asthma, or asthma with daytime and nighttime symptoms not controlled by short-acting beta2-adrenoceptor agonists
- Asthma requiring chronic use of inhaled or systemic corticosteroids
- Upper respiratory tract or sinus infection that required antibiotic therapy and had not had at least a 14-day wash-out period prior to the run-in period, or had a viral upper respiratory infection within 7 days prior to screening
- Dependence on nasal, oral or ocular decongestants, nasal topical antihistamines, or nasal steroids
- Undergoing a progressive course of immunotherapy (hyposensitization). Subjects on a regular maintenance schedule prior to the screening visit were eligible for study inclusion; however, subject could not receive hyposensitization treatment within 24 hours prior to any study visit
- Diagnosed of cancer within the past 5 years (except for successfully treated basal and squamous cell carcinomas)
- Concomitant medical problem
- Had any of the following clinical conditions: active or quiescent tuberculosis infection of the respiratory tract, untreated fungal, bacterial, systemic viral infections or ocular herpes simplex
- Smoked or had smoked within the previous 6 months
- Member of the staff, affiliated with, or family member of the staff personnel directly involved with this study
- Previously randomized into this study
- Any other clinically significant deviation from normal in the physical examination or medical history that could interfere with the study evaluation or affect subject safety
- In a situation or condition that could interfere with participation in the study
- Used any drug or device in an investigational protocol in the 30 days prior to visit 1
- Participating in other clinical studies
- Allergic or has sensitivity to the study drug or its excipients
- Compromised ability to provide informed consent
- History of non-compliance with medication or treatment protocols
Trial design
Primary purpose
Allocation
Interventional model
Masking
51 participants in 2 patient groups, including a placebo group
Trial contacts and locations
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Data sourced from clinicaltrials.gov
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