Preventing Arthritis in a Multi-Center Psoriasis At-Risk Cohort

Who is this study for? Patients with Psoriasis
What treatments are being studied? Guselkumab
Status: Recruiting
Location: See all (5) locations...
Intervention Type: Drug
Study Type: Interventional
Study Phase: Phase 4
SUMMARY

This is a multi-center (North-America), randomized, double-blind, placebo-controlled, wait-list, interventional, preventive trial of guselkumab in high-risk psoriasis patients compared to non-biologic standard of care. The primary objective of the proposed trial will be to test the hypothesis that a prolonged, unresolved skin inflammation coupled with musculoskeletal power-doppler ultrasound (MSKPDUS) abnormalities driven by IL-23 increase the risk for transition into PsA and that an intervention that targets one of these pivotal molecules (i.e., Guselkumab) will: 1. Diminish MSKPDUS findings at 24 weeks, and 2. Significantly reduce or prevent the emergence of synovio-enthesial phenotype at year 2.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• 18 years old or older;

• Both male \& female;

• Psoriasis diagnosis (per dermatologist) for at least 2 years (in at least 30% of participants);

• Willing and able to provide informed consent;

• Fulfillment of HR-PsO criteria (Psoriasis (PsO) patients will meet the definition of HR if they fulfill the following criteria: a) PsO duration \>2 years and Psoriasis Body Surface Area (BSA) \>3% and positive imaging findings in MSKPDUS defined as a RM-PsASon score of \>3.36

Locations
United States
Massachusetts
Brigham and Women's Hospital
RECRUITING
Boston
New York
NYU Langone Health
RECRUITING
New York
University of Rochester Medical Center (URMC)
RECRUITING
Rochester
Other Locations
Canada
Memorial University
RECRUITING
St. John's
Women's College Research Institute, University of Toronto
RECRUITING
Toronto
Contact Information
Primary
Jose Scher, MD
Jose.Scher@nyulangone.org
6465017400
Backup
Stephanie Eichman
Stephanie.Eichman@nyulangone.org
Time Frame
Start Date: 2022-02-16
Estimated Completion Date: 2028-07-31
Participants
Target number of participants: 176
Treatments
Experimental: Guselkumab + Topicals (GUS)
Placebo_comparator: Placebo + Topicals (PBO)
No_intervention: Standard-of-Care Therapy (SOC)
In this third, non-randomized arm, patients would continue treatment with topical therapy or UVB, as part of our ongoing natural history of disease registries. This arm will include participants fulfilling RM-PsASon criteria but also those that do not (to serve as negative controls).
Authors
Rebecca Blank, Christopher Ritchlin
Related Therapeutic Areas
Sponsors
Leads: NYU Langone Health
Collaborators: Janssen Scientific Affairs, LLC

This content was sourced from clinicaltrials.gov