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NCT07449234Terminated

A Study of Guselkumab After Switching From Ustekinumab in Participants With Moderate to Severe Psoriasis

A Non-interventional, Multi-centric, Single Country Observational Study to Assess the Safety and Effectiveness of Guselkumab After Ustekinumab (Originator or Biosimilar) in Moderate to Severe Psoriasis Patients in Clinical Routine

Source: ClinicalTrials.gov · Last updated 27 Jul 2026

Brief summary (registry, in English)

The purpose of this study is to assess the effectiveness and safety of guselkumab following a switch from ustekinumab or an ustekinumab biosimilar in participants with moderate to severe psoriasis, a chronic inflammatory skin disease characterized by erythematous, scaly plaques that may be associated with pain and pruritus, in routine clinical practice.

Status (registry)
Terminated
Study type
Observational
Enrollment
9 (actual)
First submitted
27 Feb 2026
Start date
9 Feb 2026
Primary completion date
29 Jun 2026
Lead sponsor
Janssen-Cilag Ltd.
Diseases
Psoriasis
NCT number
NCT07449234

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • Contraindication or hypersensitivity to Guselkumab or any ingredient in the injection solution/liquid

Other

  • Pregnancy or breastfeeding
  • Currently enrolled in an interventional study
  • Currently enrolled in an observational study sponsored or managed by a Janssen company

Who the study is looking for

  • Must have a confirmed diagnosis of moderate-to-severe plaque psoriasis requiring systemic treatment
  • Participants who are currently treated with Ustekinumab (either the originator or its biosimilar) and who are medically indicated to switch to Guselkumab
  • Participants who, based on the Investigator's decision, should initiate treatment with Guselkumab
  • Participants must understand and be willing and able to answer patient-reported outcomes (PROs)
  • Must sign an informed consent form (ICF) allowing data collection and source data verification in accordance with local requirements

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Save your city in your profile to sort them by distance.

SiteCityCountrySite status
Lkh-Univ. Klinikum Graz
Coordinator of this site? Confirm its status
GrazAustriaUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.