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Clinical Challenges: Early Disease in Axial Spondyloarthritis

Disease pathogenesis and onset involve an interplay between genetic and environmental factors

United statesLiron caplanNancy walshDennis mcgonagleRegina college in newportOregon health science university in portlandAssessment in spondyloarthritis international societyUniversity of leedsUniversity of coloradoSpondyloarthritis international societyAtul deodharOregon healthScience universitySalve regina college

Early axial spondyloarthritis defined as a symptom duration of less than 2 years

Early axial spondyloarthritis defined as a symptom duration of less than 2 years
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Assessment in spondyloarthritis international societyAssessment of spondyloarthritis international societyPaz universitySpondyloarthritis internationalSpondyloarthritis international society

Rinvoq Approved for Active Non-Radiographic Axial Spondyloarthritis

The FDA has approved Rinvoq (upadacitinib) for the treatment of adults with active non-radiographic axial spondyloarthritis (nr-axSpA).

Thomas hudsonAssessment in spondyloarthritis international societyDrug administrationSpondyloarthritis international societyPatient global assessmentDisease activityBath ankylosing spondylitis functional indexAnkylosing spondylitis qualityAccessed october

Bimekizumab Effective for AxSpA Regardless of Prior TNFi Use

Data after 24 weeks of treatment with bimekizumab in patients with axial spondyloarthritis show good responses overall regardless of prior experience with a tumor necrosis factor inhibitor.

Xenofon baraliakosEli lillyBristol myers squibbEuropean alliance of associationsAssessment in spondyloarthritis international societyEuropean unionRuhr university bochum germanyInternational congress on spondyloarthritidesInternational congressRuhr university bochumEuropean allianceSpondyloarthritis international societyFabian proftMedical universityNone drugAnkylosing spondylitis disease activity score

Upadacitinib Earns FDA Approval for Ankylosing Spondylitis

Janus kinase inhibitor offers oral option for patients who have failed treatment.

Assessment in spondyloarthritis international societyEuropean medicines agencyDrug administrationSpondyloarthritis international societyAnkylosing spondylitisUs food and drug administrationNited states food and drug administrationAnkylosing spondylitis bechterews diseaseRheumatoid arthritisUlcerative colitisBiologic therapyPsoriatic arthritisClinical researchClinical trialsLinical studiesHealthcare and medical technology