Another approval for the JAK blocker Rinvoq (upadacitinib) will help Chicago’s AbbVie (NYSE: ABBV) boost market share in an increasingly crowded immunology market.
The US Food and Drug Administration has granted approval for the oral therapy as a second-line option, for the treatment of certain adults with active non-radiographic axial spondyloarthritis (nr-axSpA).
Chief scientific officer Thomas Hudson said the nod provides “a new oral, once-daily treatment option for patients who historically have had limited treatment options.”
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