Observational Evaluation of Atopic Dermatitis in Pediatric Patients
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- STATUS
- Recruiting
-
- End date
- May 12, 2026
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- participants needed
- 1300
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- sponsor
- Sanofi
Summary
Primary Objectives:
- To describe the characteristics of pediatric patients with moderate to severe atopic dermatitis (AD) whose disease is not adequately controlled with topical therapies or when those therapies are not medically advisable.
- To evaluate the time-course of AD and selected atopic comorbidities.
Secondary Objectives:
- To characterize disease burden and unmet need.
- To describe real-world treatment patterns (eg, dosing regimens, treatment duration, and reasons for discontinuation and/or switching).
- To document the real-world effectiveness and safety of treatments.
Description
The study duration is 60 months.
Details
| Condition | ATOPIC DERMATITIS, eczema (atopic dermatitis), ATOPIC DERMATITIS, dermatitis, atopic, dermatitis, atopic, eczema (atopic dermatitis) |
|---|---|
| Age | 11years or below |
| Treatment | Standard of Care |
| Clinical Study Identifier | NCT03687359 |
| Sponsor | Sanofi |
| Last Modified on | 19 February 2024 |
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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