Atopic Dermatitis Registry: See how approved treatments work for adults under dermatology care
Official title: CorEvitas Atopic Dermatitis Registry: A Study of Post Approval Drug Safety and Effectiveness
Run by CorEvitas · NCT04504955 · Data updated 2026-11-12
This is a nationwide registry that follows adults with atopic dermatitis to see how safe and effective approved treatments are in real-world dermatology settings.
Quick facts
| Study type | Observational |
|---|---|
| Ages | 18 Years and up |
| Sex | All |
| Enrollment | 10000 (estimated) |
| Sponsor | CorEvitas Research network |
| Locations | 1 site (Waltham, Massachusetts) |
| Status | Recruiting |
| Started | July 14, 2020 |
| Main results expected | December 2100 |
| Study ends | December 2100 |
| Registry record updated | August 26, 2026 |
| Trial ID | NCT04504955 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Adults (18+) with a dermatologist-confirmed atopic dermatitis who are starting a new enrollment-eligible medication and able to provide informed consent and required personal information.
✕Probably not a fit
Patients who are not on a new enrollment-eligible medication or who participate without receiving any new therapy may not see direct individual benefits.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This prospective, non-interventional registry collects patient and clinician-reported data to compare the safety and effectiveness of approved atopic dermatitis therapies. It aims to describe disease course, comorbidities, treatment patterns, and patient productivity, using standardized PRO and ClinRO measures. Data are gathered in real-world clinical settings under dermatology supervision, with inclusion of adults who are newly started on an enrollment-eligible medication. The study excludes participants currently enrolled in blinded AD drug trials and relies on voluntary consent and data sharing within applicable laws.
Why it matters
Potential benefit: Participants may benefit from closer observation of treatment outcomes and contributing to knowledge that could improve future care for atopic dermatitis.
How similar studies have gone: Observational registries for atopic dermatitis have provided insights into real-world safety and effectiveness of therapies in prior work.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria Has been diagnosed with AD by a dermatologist or qualified dermatology provider. 2\) Is at least 18 years of age or older and has attained the legal age for consent to procedures involved in the research, under the applicable law of the jurisdiction in which the research is being conducted. 3\) Willing and able to provide consent for participation in the registry. 4) Willing and able to provide Personal Information (full legal name, sex, date of birth, home address zip/postal code, and email address OR phone number at a minimum) if required based on registry location and applicable laws and regulations. 5) Has been prescribed a new Enrollment Eligible Medication. A new therapy is a medication that the subject has never taken before. 1. At the time of registry enrollment OR 2. Within 12 months prior to registry enrollment Exclusion Criteria: 1)Is participating or planning to participate in a blinded clinical trial for an AD drug. Follow-Up Criteria Registry Follow-Up data collection should be done at the time of routine clinical encounters approximately every 6 months. Routine or standard of care clinical encounters may occur in between two registry visits, but the data collected in the Follow-Up forms should cover the time period since the last registry visit. For planning purposes, each Follow-Up visit is anchored to the date of the last eligible registry visit. A Follow-Up visit is eligible for payment if 150 days have passed since the last visit submission. A Follow-Up visit is not eligible for payment if conducted less than 150 days since the last registry visits except when the EARLY Follow-Up visit Criteria are satisfied. EARLY Follow-Up Criteria A registry Follow-Up visit should be conducted whenever a patient is prescribed or receiving the first dose of a new Eligible Medication even if less than 150 days have passed since the last registry visit. When the EARLY Follow-Up criteria are met, the next anticipated registry visit is calculated from the date of the Early Follow-Up visit.
Where it's running
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CorEvitas, LLC
Waltham, Massachusetts, United States Recruiting
Study contacts
- Study coordinator: Atopic Dermatitis Registry Team
- Email: ppd_coreatopicderm@thermofisher.com
- Phone: 508-408-5531
Similar studies
Other studies for the same condition or treatment. Recruiting studies are listed first.
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Roflumilast Cream 0.3% for moderate to severe atopic dermatitis in children, adolescents, and adults
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ADBest TREAT Registry for adults with atopic dermatitis
A registry in Germany is collecting real-world data from adults with atopic dermatitis to see how treatments are used and how the disease affects quality of life.
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How lebrikizumab affects the skin microbiome and mycobiome in adults with atopic dermatitis
This study looks at whether lebrikizumab changes the skin bacteria, fungi, and specifically Staphylococcus species, in adults with moderate-to-severe atopic dermatitis.
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QX-4533 safety study in healthy volunteers and people with moderate-to-severe atopic dermatitis
This study tests the safety and tolerability of QX-4533, given as a pill, in healthy adults and in patients with moderate-to-severe atopic dermatitis to see how the drug behaves in the body and what side effects may occur.
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A 52-week study will test tilrekimig against dupilumab and a placebo to see if it helps people 12 and older with moderate-to-severe atopic dermatitis.
How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.