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Clinical Trials in the USA / NCT03428646
Active, not recruiting Observational

Study of Patients Receiving DUPIXENT® for Atopic Dermatitis (AD)

NCT03428646 · tracked via the Priya Life Science USA tracker
Sponsor
Regeneron Pharmaceuticals
Phase
Observational
Started
2018-04-06
Last updated
2025-12-29

Condition(s) studied

Dermatitis, Atopic

Investigational drug(s) / intervention(s)

Dupilumab

Dupilumab: Dupixent 1 dose at Baseline required for eligibility; otherwise, no therapeutic intervention required during the course of the study. In addition to (or substituting for) DUPIXENT®, participants may receive marketed drugs as deemed necessary by their physicians for the treatment of AD or comorbid conditions.

Study summary

A long-term observational registry in patients with atopic dermatitis (AD) initiating treatment with DUPIXENT® (dupilumab)

Eligibility

Sex
ALL
Min age
12 Years
Max age
Healthy volunteers
No
Key Inclusion Criteria: * Male or female, 12 years of age or older at the baseline visit. NOTE: Adolescent patients (at least 12 years old, but less than 18 years) are eligible in the US or Canada only after DUPIXENT receives the respective country's regulatory approval for use in this age group. * Initiating treatment with DUPIXENT® as standard-of-care for AD according to the country-specific prescribing information (Note: Participants will be screened when they received their initial prescription for DUPIXENT®). * Willing and able to comply with study-related activities. * Able to understand and complete study-related questionnaires. * Provide signed informed consent or parental/legal guardian consent plus patient assent, where applicable. Key Exclusion Criteria: * Patients who have a contraindication to the drug according to the country-specific prescribing information label. * Any condition that, in the opinion of the investigator, may interfere with patient's ability to participate in the study, such as short life expectancy, substance abuse, severe cognitive impairment, or other co-morbidities that can predictably prevent the patient from adequately completing the schedule of visits and assessments. * Prior use of dupilumab within 6 months of the screening visit, or within 6 months of the baseline visit if screening and baseline occur on the same day. NOTE: Other protocol defined Inclusion/Exclusion criteria apply.

Primary outcome measure(s)

Trial sites (99)

FacilityCityRegionStatus
Regeneron Investigational Site Birmingham Alabama
Regeneron Investigational Site Gilbert Arizona
Regeneron Investigational Site Fountain Valley California
Regeneron Investigational Site Laguna Hills California
Regeneron Investigational Site Loma Linda California
Regeneron Investigational Site Los Angeles California
Regeneron Investigational Site Los Angeles California
Regeneron Investigational Site Manhattan Beach California
Regeneron Investigational Site Newport Beach California
Regeneron Investigational Site Oceanside California
Regeneron Investigational Site Redondo Beach California
Regeneron Investigational Site Riverside California
Regeneron Investigational Site Roseville California
Regeneron Investigational Site San Diego California
Regeneron Investigational Site Santa Monica California
Regeneron Investigational Site Thousand Oaks California
Regeneron Investigational Site New Haven Connecticut
Regeneron Investigational Site Coral Gables Florida
Regeneron Investigational Site Margate Florida
Regeneron Investigational Site West Palm Beach Florida
Regeneron Investigational Site Atlanta Georgia
Regeneron Investigational Site Macon Georgia
Regeneron Investigational Site Marietta Georgia
Regeneron Investigational Site Marietta Georgia
Regeneron Investigational Site Sandy Springs Georgia
Regeneron Investigational Site Champaign Illinois
Regeneron Investigational Site Chicago Illinois
Regeneron Investigational Site La Grange Park Illinois
Regeneron Investigational Site Skokie Illinois
Regeneron Investigational Site Springfield Illinois
Regeneron Investigational Site Fort Wayne Indiana
Regeneron Investigational Site Plainfield Indiana
Regeneron Investigational Site Overland Park Kansas
Regeneron Investigational Site Corbin Kentucky
Regeneron Investigational Site Louisville Kentucky
Regeneron Investigational Site Rockville Maryland
Regeneron Investigational Site Towson Maryland
Regeneron Investigational Site Upper Marlboro Maryland
Regeneron Investigational Site White Marsh Maryland
Regeneron Investigational Site Quincy Massachusetts

+ 59 more sites — see the full list on the official registry below.

On this site

📄 Dupixent (dupilumab) drug profile →

More Regeneron Pharmaceuticals trials in the USA

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT03428646 on ClinicalTrials.gov ↗ ← All trials in the USA