Treatment Effectiveness in People With axSpA or PsA Starting Treatment With Bimekizumab, Risankizumab, Guselkumab, Upadacitinib, or a TNF Inhibitor
Condition(s) studied
Investigational drug(s) / intervention(s)
observational study: This is an observational study based on existing treatments prescribed prior to inclusion. No interventions are given as part of this research.
Study summary
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.
Eligibility
Primary outcome measure(s)
- Number of participants that have achieved Low Disease Activity (LDA) at 12 months. — At 12 months
- Number of participants that have achieved Minimal Disease Activity (MDA) at 12 months. — At 12 months
- Change from baseline in PROM scores at 12 months. — At 12 months
Trial sites (1)
| Facility | City | Region | Status |
|---|---|---|---|
| Royal National Hospital for Rheumatic Diseases | Bath | Somerset | Recruiting |
Other trials for the same condition
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View NCT07166315 on ClinicalTrials.gov ↗ ← All trials in the UK