Last updated: March 10, 2022
Sponsor: Bayer
Overall Status: Completed
Phase
3
Condition
Acute Rhinitis
Common Cold
Allergy
Treatment
N/AClinical Study ID
NCT04264637
20877
Ages 18-65 All Genders Accepts Healthy Volunteers
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
- Healthy, ambulatory, male or female volunteers 18 to 65 years of age with selfreportedallergic rhinitis to ragweed pollen for at least 2 years prior.
- Documented positive skin prick test response to common ragweed (ambrosiaartemisiifolia) pollen; prick with wheal ≥3 mm larger than the diluent response atscreening or within the previous 12 months done at the research site.
- Subject is willing to abstain use of any decongestant and/or allergy medications (prescription and over-the-counter), smoking, wearing perfume and alcohol 24 hoursprior to the Qualification and Treatment Phases as instructed.
- Subject is willing to stop use of current decongestant and allergy medications at thestart of the washout period prior to qualification and during the trial as instructed.
- At the discretion of the investigator, subjects may be considered with self-reportedmild intermittent asthma (using ≤2 doses of SABA (short-acting beta agonists) perweek) or exercise-induced asthma.
- Female subjects of childbearing potential must: a) be using a medically acceptableform of birth control for at least 1 month prior to screening (3 months on oralcontraceptives); b) abstain from sexual intercourse for at least 1 month prior toscreening; or c) participate exclusively in a same sex relationship for at least 1month prior to screening. In addition, female subjects of childbearing potential musthave a negative pregnancy test at Screening and prior to entering the EnvironmentalExposure Chamber (EEC). Female subjects of non-childbearing potential must beamenorrheic for at least two years or have undergone surgical sterilization (i.e.tubal ligation/occlusion, hysterectomy and/or bilateral oophorectomy).
- At the end of the 4 hour Qualification Phase, the subject's Total Nasal Symptom Score (TNSS) via Electronic Patient Data Acquisition Tablet (ePDAT) must be ≥6 out of apossible of 12 at least twice, with at least one occurring during the last 2 timepoints to qualify to receive study intervention.
- During Treatment Phases Treatment 1 (T1) and Treatment 2 (T2), subjects are exposed topollen in EEC for a two hour induction phase. At the end of the two hour symptominduction phase during T1 and T2, subjects meet a minimum threshold total nasalsymptom score (TNSS) response of ≥6 out of a possible of 12 at least twice, with atleast one occurring during the last 2 time points to qualify to receive studyintervention.
Exclusion
Exclusion Criteria:
- Any significant medical condition which, in the judgment of the investigator, is acontraindication to the use of intranasal azelastine hydrochloride (HCl), or mightinterfere with the trial.
- Subjects with a pre-EEC TNSS ˃3 at T1.
- Subjects with a known allergy to azelastine HCl or any of its inactive ingredients, orwith a known contraindication to the use of epinephrine.
- Subjects with a known history of non-allergic rhinitis.
- Subjects with a suspected or known history of anaphylaxis to ragweed allergen.
- Subjects with a suspected or known history of rhinitis medicamentosa.
- In the judgment of the investigator, any respiratory illness or active local infection (e.g., sinusitis) prior to the Qualification Phase that can interfere with the conductof the study.
- Subjects with a known history of coronary heart disease, ischemic heart disease , highblood pressure, symptomatic prostatic hypertrophy, hepatic insufficienHas a history ofimmunological disease or malignancy within the past 5 years, with the exception ofnon-melanoma skin cancer or renal disease.
- Evidence or history of clinically significant (in the judgment of the investigator)hematological, renal, endocrine, pulmonary, gastrointestinal, cardiovascular (including hypertension), hepatic, psychiatric, neurologic diseases, or malignancieswithin the last 5 years.
- Self-reported medical history of tuberculosis, hepatitis or human immunodeficiencyvirus (HIV).
- Alcoholism or drug abuse within 2 years prior to the Screening Visit or routineconsumption of 3 or more alcohol containing beverages per day; Alcohol containingbeverages are defined as one beer (5%), one glass of wine (11%) and one shot (40%)hard liquor.
- Self-reported current heavy smokers (>1 pack/25 cigarettes per day).
Study Design
Total Participants: 110
Study Start date:
February 03, 2020
Estimated Completion Date:
March 17, 2021
Connect with a study center
Cliantha Research
Mississauga, Ontario L4W 1A4
CanadaSite Not Available
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