For Healthcare Professionals

Observational Evaluation of Atopic Dermatitis in Pediatric Patients


About the study

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.

Who can take part

You may be eligible to participate in the study if you meet the following criteria:


Inclusion criteria:

  1. Patients with moderate to severe AD, according to the Investigator's assessment;
  2. Currently receiving systemic treatment (including phototherapy) for atopic dermatitis or currently on topical treatment, but otherwise candidates for systemic treatment.


Exclusion criteria:

Concurrent participation in an interventional clinical trial which modifies patient care.

The above information is not intended to contain all considerations relevant to a patient's potential participation in a clinical trial.

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Study Locations

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How to Apply

Contact the study center to learn if this study is a good match for you.

Study’s details


Dermatitis Atopic

Age (in years)

< 11

Participants needed


Est. Completion Date

Mar 14, 2036

Treatment type

Observational [Patient Registry]


Sanofi identifier


Study number


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