Actively Recruiting
IL17 Rate and Spondyloarthritis
Led by Centre Hospitalier Universitaire de Nice · Updated on 2022-10-24
50
Participants Needed
1
Research Sites
1043 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
There are, to date, no validated biomarkers or head-to-head RCTs of biologics to guide choice of biologic agent in axSpA. While there are now two head-to-head studies of a TNF inhibitor (TNFi) vs an IL-17 inhibitor (IL-17i) in psoriatic arthritis. Recommendations refers to biological DMARDs (bDMARDs) including TNFi and IL-17i for patients with high disease activity despite the use (or intolerance/contraindication) of at least two non-steroidal anti-inflammatory drugs (NSAIDs) in axial SpA (axSpA) and in failure of a strategy including methotrexate for psoriatic arthritis. A tool to help us to decide which bDMARDs to use is necessary. In SpA, the method of determination of IL17 seems to be questionable. The determination of cytokines after stimulation of immune cells in patients with active SpA requiring a biological treatment could provide us with a tool to assist in the choice of therapy. The aim of the study was to show the feasibility of cytokine assay following lymphocyte stimulation in active SpA requiring biological treatment. And secondly, to show the predictive character of this expression on the therapeutic response at three months after the implementation of a biological treatment.
CONDITIONS
Official Title
IL17 Rate and Spondyloarthritis
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patients with spondyloarthritis meeting the ASAS criteria
- Patients planned to start biological treatment after failing at least two NSAIDs
- Active disease defined by a BASDAI score higher than 4
You will not qualify if you...
- No predominant axial symptoms
- Previous biological treatment received
- Contraindications to biological treatments
AI-Screening
AI-Powered Screening
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Trial Site Locations
Total: 1 location
1
CHU de NICE
Nice, France, 06003
Actively Recruiting
Research Team
C
Christian ROUX
CONTACT
B
Barbara SEITZ-POLSKI
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
1
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