Actively Recruiting
Comparison of Persistence of UPadacitinib vs. TNF-inhibitoRs In a German Real-world SettING
Led by AbbVie · Updated on 2026-02-17
678
Participants Needed
53
Research Sites
N/A
Total Duration
On this page
AI-Summary
What this Trial Is About
Researchers are evaluating the retention rates of two treatments, upadacitinib UPA and tumor necrosis factor inhibitors TNFi, in adults with moderate to severe active rheumatoid arthritis RA in a real-world setting in Germany. This observational study aims to compare how long patients stay on each treatment when prescribed according to local standards and labels. About 678 participants will be enrolled over approximately 24 months, with total study duration lasting up to 48 months. Participants will receive either upadacitinib or a TNFi treatment as prescribed by their physicians following local regulatory and reimbursement guidelines. The decision to treat with UPA or TNFi is made independently of the study and before recruitment. The study does not assign treatments but observes patients already prescribed these therapies. During the study, researchers will monitor participants for up to 24 months to measure retention rates of the treatments. Data collection will include regular assessments according to routine care practices to track treatment persistence. The study focuses on real-world outcomes without altering standard treatment or care. Safety monitoring and follow-up will be conducted as part of usual medical care.
CONDITIONS
Brief Title
A Comparison Study of Persistence of UPadacitinib vs. TNF-inhibitoRs In a German Real-world SettING
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Current or past diagnosis of moderate to severe active rheumatoid arthritis as confirmed by a physician
- Treatment decision with upadacitinib or tumor necrosis factor inhibitor made before study recruitment
- Upadacitinib or TNFi prescribed according to approved label and local policies
You will not qualify if you...
- Participation in a clinical trial with an investigational drug within at least 30 days or 5 half-lives before baseline
- Prior treatment with upadacitinib
- Prior treatment with the same tumor necrosis factor inhibitor prescribed for this study
Research Team
M
Medical Information Germany
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