🔎 Trials Near Me

Home › Atopic Dermatitis (Eczema) › NCT07290803

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

RecruitingObservational study

Atopic Dermatitis Disease Registry of Adult and Adolescent Patients Initiating or Switching Systemic Treatments

Who can join

Ages 12 and older · All sexes

Full eligibility criteria
Inclusion Criteria:

* 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.

Exclusion Criteria:

* 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.

About the 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 · Participants: 1,000 · Started: Nov 17, 2025

Contact the study team

Official record on ClinicalTrials.gov — NCT07290803

Locations in the U.S.

AlabamaCahaba Dermatology & Skin Health Center- Site Number : 8400006, Birmingham
River Region Dermatology and Laser- Site Number : 8400041, Montgomery
ArizonaSan Tan Allergy & Asthma- Site Number : 8400031, Gilbert
Saguaro Dermatology- Site Number : 8400028, Phoenix
CaliforniaKern Research, Inc.- Site Number : 8400047, Bakersfield
Center for Dermatology Clinical Research- Site Number : 8400014, Fremont
Dermatology Research Associates - Los Angeles- Site Number : 8400020, Los Angeles
Northridge Clinical Trials, LLC- Site Number : 8400009, Northridge
Sunwise Clinical Research, LLC.- Site Number : 8400010, Oakland
Empire Clinical Research, LLC- Site Number : 8400007, Pomona
University Clinical Trials- Site Number : 8400019, San Diego
ColoradoWestern States Clinical Research, Inc.- Site Number : 8400051, Wheat Ridge
FloridaSt. Jude Clinical Research- Site Number : 8400049, Doral
Ziaderm Research, LLC- Site Number : 8400021, North Miami Beach
GeorgiaSkin Care Physicians of Georgia - Macon- Site Number : 8400034, Macon
IllinoisSneeze, Wheeze, & Itch Associates, LLC- Site Number : 8400029, Normal
Rosalind Franklin University of Medicine and Science- Site Number: 8400056, North Chicago
MichiganDavid Fivenson, MD, Dermatology, PLLC- Site Number : 8400017, Ann Arbor
Oakland Hills Dermatology- Site Number : 8400042, Auburn Hills
Great Lakes Research Group - Bay City- Site Number : 8400052, Bay City
The Derm Institute of West Michigan- Site Number : 8400025, Caledonia
Wayne State University - Detroit Medical Center- Site Number : 8400035, Detroit
Michigan Dermatology Institute - Waterford- Site Number : 8400013, Waterford
MissouriRed River Research Partners, Llc- Site Number : 8400054, Bolivar
Cleaver Dermatology- Site Number : 8400033, Kirksville
NebraskaAllergy Asthma & Immunology- Site Number : 8400044, Lincoln
NevadaLas Vegas Dermatology- Site Number : 8400002, Las Vegas
New HampshireOptima Research Portsmouth- Site Number : 8400032, Portsmouth
New MexicoUniversity Of New Mexico School Of Medicine- Site Number : 8400022, Albuquerque
North CarolinaPiedmont Plastic Surgery and Dermatology- Site Number : 8400038, Huntersville
Wake Forest University Health Sciences- Site Number : 8400003, Winston-Salem
North DakotaRed River Research Partners - Fargo- Site Number : 8400037, Fargo
OhioDermatology Associates of Mid-Ohio- Site Number : 8400026, Marion
Dermatologists of Southwest Ohio - Mason- Site Number : 8400050, Mason
PennsylvaniaUPMC - Department of Dermatology- Site Number : 8400024, Pittsburgh
Rhode IslandCare Access Research - Warwick 2- Site Number : 8400045, Warwick
South CarolinaAdvanced Dermatology and Cosmetic Surgery - Spartanburg- Site Number : 8400004, Spartanburg
TexasReveal Research Institute - Dallas- Site Number : 8400012, Dallas
Austin Institute for Clinical Research, Inc- Site Number : 8400030, Pflugerville
Complete Dermatology - Sugar Land- Site Number : 8400001, Sugar Land
UtahCope Family Medicine - Ogden Clinic- Site Number : 8400053, Bountiful
Springville Dermatology - Springville- Site Number : 8400055, Springville
VirginiaFuchs Dermatology- Site Number : 8400027, Falls Church
WashingtonFrontier Dermatology Partners CRO LLC- Site Number : 8400011, Mill Creek
University of Washington - Roosevelt Location- Site Number : 8400005, Seattle

Conditions

From ClinicalTrials.gov, data retrieved Sep 30, 2026. Each study sets its own eligibility; the study team decides who can join.