Clinical trial Recruiting at 1 site Observational Ages 18 and up

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.

More Atopic Dermatitis trials

Quick facts

Study typeObservational
Ages18 Years and up
SexAll
Enrollment10000 (estimated)
SponsorCorEvitas
Research network
Locations1 site (Waltham, Massachusetts)
StatusRecruiting
StartedJuly 14, 2020
Main results expectedDecember 2100
Study endsDecember 2100
Registry record updatedAugust 26, 2026
Trial IDNCT04504955 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

  • CorEvitas, LLC
    Waltham, Massachusetts, United States
    Recruiting

Study contacts

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.