RecruitingNCT05744466

A Real-world Observational Study to Compare Effectiveness of Deucravacitinib Vs Apremilast in Adults With Plaque Psoriasis

A Real-world, Prospective, Observational Study of the Comparative Effectiveness of Deucravacitinib Versus Apremilast in Adults With Plaque Psoriasis - North American Region


Sponsor

Bristol-Myers Squibb

Enrollment

1,500 participants

Start Date

Sep 30, 2022

Study Type

OBSERVATIONAL

Conditions

Summary

The purpose of this study is to understand the comparative effectiveness of deucravacitinib versus apremilast in adults with plaque psoriasis.


Eligibility

Min Age: 18 Years

Inclusion Criteria3

  • Have been diagnosed with plaque psoriasis by a dermatologist
  • Newly initiating an eligible medication for enrollment (i.e., deucravacitinib, apremilast)
  • Actively enrolled in the CorEvitas Psoriasis Registry and have documented consent to allow copies of information from the registry be used for research purposes

Exclusion Criteria2

  • Participation (current or planned) in an interventional clinical trial (does not include observational registry or study)
  • Restart of treatments with the study eligible therapies previously received at any time during the participants' treatment history

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Interventions

DRUGDeucravacitinib

As prescribed by treating clinician

DRUGApremilast

As prescribed by treating clinician


Locations(1)

Local Institution

Waltham, Massachusetts, United States

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NCT05744466


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