Clinical trial Recruiting at 1 site Observational Ages 18 and up

Psoriasis patients starting or switching systemic therapy: safety and real-world outcomes

Official title: CorEvitas Psoriasis (PSO) Registry

Run by CorEvitas · NCT02707341 · Data updated 2026-11-12

This registry tests the safety of approved psoriasis medicines in adults treated by dermatologists in North America.

Quick facts

Study typeObservational
Ages18 Years and up
SexAll
Enrollment10000 (estimated)
SponsorCorEvitas
Research network
Drugs / interventionssecukinumab
Locations1 site (Waltham, Massachusetts)
StatusRecruiting
StartedApril 2015
Main results expectedDecember 2100
Study endsDecember 2100
Registry record updatedAugust 27, 2026
Trial IDNCT02707341 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Adults (18+) with dermatologist-diagnosed psoriasis who recently started or switched to a systemic psoriasis therapy within the last 12 months and can provide consent and identifiable information.

Probably not a fit

Patients not receiving systemic therapy or not willing to participate or provide consent/PII may not benefit from participation.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

The CorEvitas Psoriasis Registry collects real-world data from approximately 200 North American sites to monitor safety, including adverse events of special interest like malignancy, among adults with moderate to severe plaque psoriasis on systemic or biologic therapies. It features a parallel structure modeled after the Corrona RA Registry and is co-managed by Corrona, LLC and the National Psoriasis Foundation. Patients who recently started or switched systemic psoriasis treatment can enroll, with data collected as part of routine care under physician supervision. All treatments are standard-of-care and decisions remain with the treating physician. Study procedures involve observational data collection without a specified interventional protocol.

Why it matters

Potential benefit: If successful, the registry could clarify safety profiles and inform treatment decisions for psoriasis therapies in real-world practice.

How similar studies have gone: Other large observational registries, including the Corrona RA Registry framework, have provided meaningful real-world safety and practice-pattern insights.

Who can join: the full rules

Show full inclusion / exclusion criteria
ELIGIBILITY CRITERIA∗ To be eligible for enrollment into the CorEvitas Psoriasis Registry, a patient must satisfy all of the inclusion criteria and none of the exclusion criteria listed below.

Inclusion Criteria:

The patient must:

1. Have been diagnosed with psoriasis by a dermatologist.
2. Be at least 18 years of age or older.
3. Be willing and able to provide written consent for participation in the registry.
4. Be willing and able to provide Personally Identifiable Information (PII) that includes the following types of personal information at a minimum: 1) Full Name and 2) Date of Birth.
5. Meet one of the following criteria.

Have started on or switched to a systemic psoriasis treatment within the previous 12 months†▲:

Exclusion Criteria:

1\. Patient is participating in or planning to participate in a double-blind randomized of a psoriasis drug. Of note, concurrent participation in another observational registry or open-label Phase 3b/4 trial is not excluded.

Where it's running

  • 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.