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Study identifier: NCT07166315 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Treatment Effectiveness in People With axSpA or PsA Starting Treatment With Bimekizumab, Risankizumab, Guselkumab, Upadacitinib, or a TNF Inhibitor

Condition: Axial Spondylarthritis (axSpA) · Psoriatic Arthritis (PsA)  ·  Sponsor: Adelphi Real World

PhaseN/A
Planned participants700
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

This observational study will target patients with axial spondyloarthritis (axSpA) and psoriatic arthritis (PsA) who have started treatment with bimekizumab, upadacitinib, risankizumab, guselkumab, or a tumour necrosis factor-alpha inhibitor (e.g., adalimumab or etanercept) at NHS hospitals in the United Kingdom. Information from patients' medical records will be collected, and patients will complete surveys about their experiences with their treatment. The study will look at treatment effectiveness from both healthcare professionals' and patients' points of view.

This description comes directly from the study's public registry record.

Talk to the study team

SpA Extend Team  ·  +441625 577 829  ·  arwspaextend@adelphigroup.com

Always discuss trial participation with your own doctor first.

Locations (1)

Royal National Hospital for Rheumatic DiseasesBath, Somerset, United KingdomRecruiting

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Source record: clinicaltrials.gov/study/NCT07166315