Treatment Effectiveness in People With axSpA or PsA Starting Treatment With Bimekizumab, Risankizumab, Guselkumab, Upadacitinib, or a TNF Inhibitor
Eligible age
18+ yrs
Accepts
All genders
Locations
0 states
Healthy volunteers
No
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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.
Sponsor: Adelphi Real World
You may qualify if…
- ✓ Participant has a clinical diagnosis of axial spondyloarthritis (axSpA) or psoriatic arthritis (PsA).
- ✓ Participant has been prescribed advanced therapy within one month prior to enrolment in the study, to treat their axSpA or PsA.
- ✓ Participant is aged 18 years or older at enrolment.
You may not qualify if…
- ✕ Participation in a clinical trial at enrolment.
Source: ClinicalTrials.gov · NCT07166315 · last updated 2026-10-27