NCT05922891Completed
Tezepelumab PRO Study
Effectiveness of Tezepelumab on Asthma Control and Cough: A Prospective, Multi-center, Observational Study
Source: ClinicalTrials.gov · Last updated 21 Aug 2026
Brief summary (registry, in English)
This study assesses the impact of tezepelumab treatment not only on asthma control but also on cough specific Health-Related Quality of Life (HRQoL). Asthma control can be evaluated using Asthma Control Questionnaire (ACQ). Cough symptom which is one of the symptoms related airway hyperresponsiveness can be assessed via the relevant questionnaire, Leicester Cough Questionnaire (LCQ). There is moderate negative correlation between ACQ and LCQ . Improvements in both asthma control and cough symptom by tezepelumab would clarify effectiveness of Tezepelumab in real-world. Though Tezepelumab is recently approved in Japan, there is no real-world evidence on tezepelumab, particularly on above mentioned symptoms. Thus, this study aims to estimate effectiveness of tezepelumab on asthma and cough symptoms in real world settings.
- Status (registry)
- Completed
- Study type
- Observational
- Enrollment
- 92 (actual)
- First submitted
- 20 Jun 2023
- Start date
- 27 Sept 2023
- Primary completion date
- 20 Sept 2025
- Lead sponsor
- AstraZeneca
- Diseases
- Asthma
- NCT number
- NCT05922891
What you commit to
- Study type: Observational
- Participants enrolled: 92
- From 27 Sept 2023 to the primary completion date, 20 Sept 2025
- 29 sites in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Prior treatment
- Patients who had asthma exacerbation within one month before study enrollment
- Patients who had the biologics treatment in following period prior to the enrollment
- omalizumab in 2 or 4 weeks depending on the body weight and total IgE amount
- mepolizumab in 4 weeks
- Benralizumab in 8 weeks
- Dupilumab in 2 weeks
Other illness
- Patients with cough related diseases other than asthma as determined by treating physicians
- Patients participating in studies that affect this study (study with other interventional treatment to evaluate efficacy/safety of treatment in patients with cough, asthma, or allergic/eosinophilic diseases)
- Any disorder, including heart failure, malignancy, morbid obesity(BMI≧35) , respiratory infectious disease that is not stable (e.g. patients who need medical treatment) in the opinion of the investigator and could:
- Affect the safety of the patient throughout the study
- Impede the patient's ability to complete the entire duration of study
Other
- Patients with pregnancy or lactation period
Who the study is looking for
- Patients aged ≥18 years who provide informed consent and who receive new prescription of Tezepelumab as per the physician's decision at baseline according to the package insert saying "Tezepelumab is given to patient with asthma (limited to severe or refractory patient whose asthma symptoms cannot be controlled even with existing treatment)"
- ACQ-6 ≥1.5 at baseline
- Patients with persistent cough ≥8 weeks up until the baseline visit according to The Japanese Respiratory Society Guidelines for the Management of Cough and Sputum 2019
Age in the registry: 18 years to 130 years · Sex: All · Does not accept healthy volunteers
Sites (29)
Sites in registry order. Pick your city on the disease page to sort them by distance.
This page is information, not medical advice. Discuss any trial with your doctor.