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Clinical Trial Summary

Primary Objective: To characterize the patients who receive Dupixent® (dupilumab) for AD in a real-world setting, with respect to their medical history, socio-demographic and disease characteristics, and prior and concomitant treatments of AD Secondary Objectives: - To characterize real-world use patterns of Dupixent® for AD (eg, used regimens, reason for initiation of new treatments, concomitant therapies, treatment durations and reasons for discontinuation and/or switching) - To assess the long-term effectiveness of Dupixent® in AD patients in a real-world setting - To assess comorbid atopic conditions and effects of treatment in comorbid atopic conditions in patients who receive Dupixent® for AD - To collect safety data on study participants


Clinical Trial Description

Participants enrolled in the study will be followed for 5 years. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03992417
Study type Observational [Patient Registry]
Source Sanofi
Contact
Status Active, not recruiting
Phase
Start date June 11, 2019
Completion date March 31, 2027

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