Actively Recruiting

Age: 18Years - 90Years
All Genders
NCT05592574

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

Age: 18Years - 90Years
All Genders

Eligibility Criteria

Eligible

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
Not Eligible

You will not qualify if you...

  • No predominant axial symptoms
  • Previous biological treatment received
  • Contraindications to biological treatments

AI-Screening

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Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

CHU de NICE

Nice, France, 06003

Actively Recruiting

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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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