AbbVie Inc. obtained its second approval in 2019 of an autoimmune therapy intended to help replace revenue from biosimilar-threatened Humira, as the US Food and Drug Administration okayed Rinvoq (upadacitinib) on 16 August to treat patients with moderately to severely active rheumatoid arthritis who have had inadequate responses to or cannot tolerate methotrexate.
The Chicago-area pharma is reportedly pricing the once-daily oral Janus kinase 1 (JAK1) inhibitor at $59,000 a year, and it...







