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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
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.
Age
18 - No limit years
Sex
ALL
Healthy Volunteers
No
LKH-Univ. Klinikum Graz
Graz, Austria
Start Date
February 9, 2026
Primary Completion Date
March 15, 2027
Completion Date
September 1, 2027
Last Updated
March 13, 2026
200
ESTIMATED participants
Lead Sponsor
Janssen-Cilag Ltd.
NCT07116967
NCT07250802
NCT07449702
Data Source & Attribution
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