For Healthcare Professionals

Observational Evaluation of Atopic Dermatitis in Pediatric Patients

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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.
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Who can take part

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

INCLUSION 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

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

Enter your ZIP code/Postal code/PIN code to locate study sites near you:

How to Apply


Contact the study center to learn if this study is a good match for you.
Phone iconCall 800-633-1610Email iconEmail Study Center

Study Details


Contition

Dermatitis Atopic

Participants Needed

1856

Est. Completion Date

Apr 21, 2036

Treatment Type

OBSERVATIONAL


Sponsor

Sanofi

ClinicalTrials.gov NCT Identifier

NCT03687359

Study Number

OBS15333

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