Description of Characteristics, Such as Age, Previous and Concurrent Treatments, Associated Diseases, of Patients With Asthma Treated With Dupilumab (DUPIXENT) (REVEAL)
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- STATUS
- Recruiting
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- End date
- Dec 21, 2026
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- participants needed
- 800
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- sponsor
- Sanofi
Summary
- To characterize real-world use patterns of DUPIXENT for asthma (eg, most commonly used regimens, reason for initiation of new asthma treatments, concomitant therapies, treatment durations, and reasons for discontinuation and/or switching)
- To assess the effectiveness of DUPIXENT in asthma patients in a real world setting (lung function improvement, exacerbation rate, asthma control)
- To assess comorbid type 2 conditions (atopic/allergic) and patterns of use and effects of treatment in comorbid conditions in asthma patients treated with Dupixent
- To collect data on HealthCare Resource Utilization (HCRU)
- To collect safety data on study participants in the real-world setting.
Description
Details
Condition | Asthma |
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Age | 12years or above |
Treatment | Dupilumab SAR231893 |
Clinical Study Identifier | NCT04550962 |
Sponsor | Sanofi |
Last Modified on | 8 December 2023 |
Eligibility
How to participate?
Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.
Learn moreIf you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.
Learn moreComplete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.
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