Clinical Characteristics, Treatment Patterns and Outcomes in Patients With axSpA and PsA Following Initiation of Bimekizumab, Risankizumab, Guselkumab, Upadacitinib or a TNF Inhibitor

Status: Recruiting
Location: See location...
Intervention Type: Other
Study Type: Observational
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
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• 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.

Locations
Other Locations
United Kingdom
Royal National Hospital for Rheumatic Diseases
RECRUITING
Bath
Contact Information
Primary
SpA Extend Team
arwspaextend@adelphigroup.com
+441625 577 829
Time Frame
Start Date: 2025-07-07
Estimated Completion Date: 2027-03
Participants
Target number of participants: 700
Treatments
Axial spondyloarthritis (axSpA)
Patients diagnosed with axial spondyloarthritis (axSpA) who are initiating treatment with bimekizumab, upadacitinib, or a tumour necrosis factor-alpha inhibitor.
Psoriatic arthritis (PsA)
Patients diagnosed with psoriatic arthritis (PsA) who are initiating treatment with bimekizumab, upadacitinib, risankizumab, guselkumab or a tumour necrosis factor-alpha inhibitor.
Sponsors
Leads: Adelphi Real World

This content was sourced from clinicaltrials.gov