Guselkumab vs Golimumab in PsA TNF Inadequate Responder Patients A Pragmatic Trial (EVOLUTION).

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Guselkumab vs Golimumab in PsA TNF Inadequate Responder Patients A Pragmatic Trial (EVOLUTION).

Brief description of study

This research study is being conducted to determine whether switching to an IL23 inhibitor (guselkumab) is more effective than switching to a second TNFi (golimumab) for patients with PsA who had an inadequate response to a TNFi. Guselkumab and Golimumab are prescription medicines that have been approved by the U.S. Food and Drug Administration (FDA) for the treatment of active psoriatic arthritis in adults. You may be eligible to receive the medication without participation in this study. This study will also investigate whether determine whether more frequent dosing of GUS (every 4 weeks), a higher dose than the currently approved dose, is more effective than GUS every 8 weeks (the currently approved dosing).

Clinical Study Identifier: s23-00181

ClinicalTrials.gov Identifier: NCT05669833

Principal Investigator: Soumya M Reddy.

Other Investigators: Rebecca Haberman, Rebecca Barbara Blank.

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