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The FDA will not meet action dates for AbbVie Inc’s (NYSE:ABBV) supplemental marketing applications for Rinvoq (upadacitinib) for active psoriatic arthritis and adults with active ankylosing spondylitis. The FDA cited its ongoing review of Pfizer Inc’s (NYSE:PFE) post-marketing study, ORAL Surveillance, evaluating tofacitinib in patients with rheumatoid arthritis.
...read full article on Benzinga
