RecruitingAtopic Dermatitis

This Study is a Non-interventional Disease Registry of Adolescent and Adult Patients With Atopic Dermatitis Who Initiate or Switch Any Systemic Treatment

Eligible age

12+ yrs

Accepts

All genders

Locations

23 states

Healthy volunteers

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About this study

The objectives of this prospective non-interventional study are to characterize the existing unmet needs across the spectrum of atopic dermatitis (AD), enhance the understanding of the patient journey, and evaluate the safety and clinical outcomes of systemic AD treatments in a real-world setting. Additionally, patient-specific factors (such as age, skin color, AD flare triggers, previous treatment responses, comorbid conditions, and the extent and site of lesions) will be assessed to better characterize the impact on the treatment journey across a broad age range and diverse geographic regions. The study will be conducted across 10 countries in 4 different geographical regions, with a follow-up period of 5 years.

Sponsor: Sanofi

You may qualify if…

✓ Patients aged more than or equal to (≥) 12 years at the time of consent.
✓ Confirmed diagnosis of AD, of any severity, according to the Investigator's assessment as aligned with International Classification of Diseases 10th revision (ICD-10) code of L20.
✓ Prescribed and scheduled to initiate any systemic treatment for AD (including but not limited to biologics, oral Janus kinase (JAK) inhibitors, cyclosporine, azathioprine, methotrexate, mycophenolate mofetil)
✓ Signed informed consent for registry participation by the patient or parent/legal representative and assent by the patient appropriate to the patient's age, including willingness to participate in long-term follow-up.

You may not qualify if…

✕ Concurrent participation in an interventional clinical trial that administers an investigational drug that modifies patient care.
✕ Insufficient understanding of the study by the patient and/or parent/guardian.
✕ The above information is not intended to contain all considerations relevant to a patient's potential participation in a clinical trial.