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Study identifier: NCT05592574 Synced from ClinicalTrials.gov · July 28, 2026
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IL17 Rate and Spondyloarthritis

Condition: Spondylarthritis  ·  Sponsor: Centre Hospitalier Universitaire de Nice

PhaseN/A
Planned participants50
Who can joinAll sexes, 18 Years to 90 Years
Healthy volunteersNo

About this study

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.

This description comes directly from the study's public registry record.

Talk to the study team

Christian ROUX  ·  +33492035491  ·  roux.c2@chu-nice.fr

Barbara SEITZ-POLSKI  ·  +33492035990  ·  seitz-polski.b@chu-nice.fr

Always discuss trial participation with your own doctor first.

Locations (1)

CHU de NICENice, FranceRecruiting

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Source record: clinicaltrials.gov/study/NCT05592574