Tezepelumab in Allergic Rhinitis and Asthma Study (TEZARS)

Phase

Condition

Common Cold

Allergy

Nasal Obstruction

Treatment

Tezepelumab

Clinical Study ID

NCT06189742

TEZARS-001

Ages 18-65
All Genders
Accepts Healthy Volunteers

Study Summary

The goal of this clinical trial is to learn about how well tezepelumab (pronounced TEZ e PEL ue mab), a Health Canada-approved drug for severe asthma, works in participants with coexisting allergic asthma and allergic rhinitis (hayfever). The main questions it aims to answer are:

How well does the study drug work to reduce nasal symptoms following exposure to an allergen after 6 doses, and after 12 doses?
Does the study drug reduce chemicals found in the nose known to be involved in the allergic rhinitis response?

Both allergic and non-allergic participants will be enrolled in the study.

Non-allergic participants will:

Not be receiving the study drug.
Be exposed to allergen via the Nasal Allergen Challenge, which involves the administration of allergen extract directly to the nose.
Complete nasal symptom and quality of life questionnaires
Have nasal fluid and blood samples collected at various time points up to 24 hours following allergen exposure.
Visit the clinic 3 separate times:
- At a screening visit to determine their eligibility to participate in the study
- At the baseline Nasal Allergen Challenge visit
- At the 24-hour post-Nasal Allergen Challenge follow-up visit

Allergic participants will:

Receive one dose of tezepelumab every 1 month for 12 months. Tezepelumab will be administered as an injection into the fatty layer just beneath the skin on the stomach, arm, or thigh.
Be exposed to allergen via the Nasal Allergen Challenge, which involves the administration of allergen extract directly to the nose.
Complete nasal symptom and quality of life questionnaires
Have nasal fluid and blood samples collected at various time points up to 24 hours following allergen exposure.
Visit the clinic 17 separate times:
- At a screening visit to determine their eligibility to participate in the study
- At the baseline, 6-month, and 12-month Nasal Allergen Challenge visits
- At each 24-hour post-Nasal Allergen Challenge follow-up visit
- For each dose of the study drug

The investigator will compare changes in nasal symptoms and allergic chemicals measured from nasal fluid and blood samples between non-allergic participants and allergic participants at baseline and at 6- and 12-months following the use of the study drug.

Eligibility Criteria

Inclusion

Inclusion Criteria:

For inclusion in the study, all participants should fulfil the following criteria based on local regulations:

Must be able and willing to provide written informed consent.
Must be willing and able to comply with the study requirements.
People between the ages of 18 and 65.
Body weight greater than 45 kg.
A person of childbearing potential must be either abstinent or using a medicallyacceptable method of birth control (see Section 3.5) and produce a negative urinepregnancy test at the screening visit and again at each treatment visit. For inclusion in the study, non-allergic participants should fulfil the followingadditional criteria based on local regulations:
Negative skin prick test to all relevant aeroallergen at screening with a whealdiameter no larger than that produced by the negative control.
Specific IgE levels to a relevant allergen are undetectable.
Negative screening Nasal Allergen Challenge, defined by a TNSS response of ≤ 3 (on a 12-point scale) and a decrease in PNIF of ≤ 30% after 10 minutes in response to anasal application of a relevant aeroallergen extract. For inclusion in the study, allergic participants should fulfil the followingadditional criteria based on local regulations:
A minimum 2-year documented history of rhinoconjunctivitis symptoms to a relevantaeroallergen.
Positive skin prick test to a relevant aeroallergen at screening (matching thehistory in IC2) with a wheal diameter at least 5 mm larger than that produced by thenegative control.
A minimum 2-year documented history of asthma, controlled with either moderate orhigh dose inhaled corticosteroids with or without another controller medication (long-acting beta-agonists and/or montelukast and/or a long-acting muscarinicantagonist.
Positive screening Nasal Allergen Challenge, defined by a TNSS response of ≥ 7 (on a 12-point scale) and a decrease in PNIF of ≥ 50% after 10 minutes in response to anasal application of a relevant aeroallergen extract.

Exclusion

Exclusion Criteria:

Participants should not enter the study if any of the following exclusion criteria are fulfilled:

Involvement in the planning and/or conduct of the study (applies to bothInvestigator staff and/or staff at the study site).
Is unlikely to cooperate with the requirements of the study including having theability to communicate with the investigator appropriately.
Inability to attend study visits or adhere to the study protocol, in the judgment ofthe principal investigator.
Previous enrolment in the present study.
Participation in another clinical study with an investigational product during thelast 30 days.
Known hypersensitivity to the investigational product.
Currently uses or is expected to use any of the prohibited medications or othertreatments as listed in Section 7.7.
An upper respiratory tract infection within 14 days of the NAC portion of thescreening visit or baseline NAC visit.
History of immunological disorders or other diseases (including, but not limited tomalignancy, cardiovascular, gastrointestinal, hepatic, renal, haematological,neurological, endocrine or pulmonary disease) that in the opinion of theinvestigator may pose additional risk factors for participation. Participants withbasal cell carcinoma or squamous cell carcinoma that has been excised in the past 5years may still participate in the study.
Nasal conditions that, according to the opinion of the investigator, may affect theoutcome of the study, i.e. nasal septal perforation, current nasal polyps, othernasal malformations or history of frequent nosebleeds.
A known history of positive test results for Hepatitis B, Hepatitis C, HIV ortuberculosis other than what would be anticipated following vaccination.
Participant has a known history of current or previous parasitic infection.
Participant that is pregnant, lactating or actively trying to become pregnant.
Participant with a clinically relevant abnormality on physical examination.
Participant is unable to communicate or to understand the requirements of the study,which would impair communication between the participant and the investigator.
Significant history of alcohol or drug abuse, in the judgment of the investigator.
Serious asthma exacerbation requiring a hospital visit and/ or treatment with oralsteroids within 4 weeks prior to screening.
FEV1 < 40 % predicted at screening.
Pre-NAC TNSS > 4 at the screening and baseline NAC visit.

Study Design

Tezepelumab

January 29, 2024

April 30, 2026

Study Description

Tezepelumab is a novel monoclonal antibody that blocks thymic stromal lymphopoietin (TSLP), a molecule implicated in allergic disease. The purpose of this open-label, unblinded, exploratory mechanistic pilot study will be to evaluate the efficacy of tezepelumab (1 subcutaneous injection of 210mg given once every 4 weeks) in participants with moderate to severe allergic asthma and concomitant seasonal and perennial AR (SAR and/or PAR) over 12 months.

The tezepelumab in allergic rhinitis and asthma study (TEZARS) is a single-centre study. The trial will enrol 14 non-pregnant/non-lactating female and/or male comorbid allergic rhinitis (AR) and allergic asthma participants ages 18 to 65 years old from the Kingston, Frontenac, Lennox and Addington regions. An additional 5 non-allergic participants will be enrolled to participate in the baseline Nasal Allergen Challenge (NAC) visit and then will exit the study. Comorbid AR and allergic asthma participants attend the baseline NAC, then receive one dose of tezepelumab every 1 month for 12 months. A 6-month post-treatment follow-up NAC will be conducted one month following the sixth dose. A 12-month post-treatment follow-up NAC will be conducted two weeks following the twelfth dose. At each NAC visit, symptom scores and quality of life questionnaires, in addition to nasal fluid and blood samples will be collected at various time points.

The investigators hypothesize that tezepelumab will improve AR-related outcomes (TNSS; Peak Nasal Inspiratory Flow, PNIF; Rhinitis Control Assessment Test, RCAT) that are stimulated by NAC with seasonal and perennial allergens in our study population. Secondarily, the investigators hypothesize tezepelumab will decrease the release of allergic mediators (i.e., IL-1b, IL-3, IL-4, IL-5, IL-6, IL-8, IL-9 IL-10, IL-13, IL-18, MCP-1, TNFα, RANTES, eotaxin, tryptase, chymase) and alarmins (i.e., TSLP, IL-25, and IL-33) in the nose following NAC. A decrease in the gene expression of TSLP and mast cell mediators (tryptase and chymase) is also anticipated. Furthermore, the number of both nasal and peripheral eosinophils and total and specific immunoglobulin E (IgE) following NAC will decline after tezepelumab treatment. Five non-atopic controls will undergo baseline NAC to confirm the reliability of allergic mediator and alarmin methodologies. The investigators also hypothesize asthma-related outcomes (spirometry; Fractional Exhaled Nitric Oxide, FeNO; Asthma Control Questionnaire 5, ACQ5) will improve following treatment with tezepelumab. Finally, the NAC protocol in an asthmatic population will be assessed.

Connect with a study center

Kingston Health Sciences Centre- Kingston General Hospital
Kingston, Ontario K7L 2V7
Canada
Active - Recruiting

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