AbbVie Announces New Drug Application Accepted for Priority Review by U.S. FDA for Upadacitinib for Treatment of Moderate to Severe Rheumatoid Arthritis

PRNewswire

Feb 19, 2019

- Upadacitinib, an investigational once-daily oral JAK1-selective inhibitor, is being studied for the treatment of adult patients with moderate to severe rheumatoid arthritis[1-8]

- The New Drug Application (NDA) is supported by data from the global upadacitinib SELECT Phase 3 program evaluating more than 4,000 patients with moderate to severe rheumatoid arthritis[3-7]

- AbbVie used a priority review voucher to expedite review of the upadacitinib NDA

PR Newswire

NORTH CHICAGO, Ill., Feb. 19, 2019

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