Residual Exacerbations With Mepolizumab
Type and Mechanisms of Residual Asthma Exacerbations in Patients Treated With Mepolizumab
Laval University
60 participants
Jul 6, 2021
OBSERVATIONAL
Conditions
Summary
This will be a two-year prospective study to characterize the nature of the remaining asthma exacerbations in patients treated with mepolizumab. Participants will be assessed every six months from pre- until two years of treatment in addition to whenever they experience an exacerbation of asthma during the study period. During these visits, various clinical, physiological and inflammatory outcomes will be assessed.
Eligibility
Inclusion Criteria3
- With a proven diagnosis of severe asthma as defined by the Canadian Thoracic Society
- Eligible for mepolizumab treatment
- Able and willing to sign the informed consent form
Exclusion Criteria2
- Any respiratory disease apart from asthma
- Confounding comorbidities sur as eosinophilic granulomatosis with polyangiitis (EGPA) or hypereosinophilic syndrome
Interventions
100 mg subcutaneous injections every four weeks
Locations(1)
View Full Details on ClinicalTrials.gov
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NCT04578171