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The principal end-point ended up being 40% improvement in infection activity according to the Assessment of SpondyloArthritis international community (ASAS4 criteria at few days 16 (in the LD group) and at week 52 (within the NL group) in tumefaction necrosis aspect inhibitor (TNFi)-naive patients. Safety anined improvement in symptoms of nonradiographic axial SpA through 52 days. Security was in ke
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