AbbVie Announces Extension of Review for Supplemental New Drug Application of Upadacitinib for the Treatment of Adults with Active Psoriatic Arthritis
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NORTH CHICAGO, Ill., March 17, 2021 /PRNewswire/ AbbVie (NYSE:ABBV), a global research and development-based biopharmaceutical company, announced that the U.S. Food and Drug Administration (FDA) has extended the review period for the supplemental New Drug Application (sNDA) for upadacitinib in the treatment of adult patients with active psoriatic arthritis. The updated Prescription Drug User Fee Act (PDUFA) action date has been extended three months to late Q2 2021.
AbbVie recently received an information request from the FDA for an updated assessment of the benefit-risk profile for upadacitinib in psoriatic arthritis. AbbVie responded to the request and the FDA will require additional time for a full review of the submission.
AbbVie: FDA Extends Review Period For SNDA Of Upadacitinib To Q2
WASHINGTON (dpa-AFX) - AbbVie (ABBV) said Wednesday that the U.S. Food and Drug Administration has extended the review period for the supplemental New Drug Application or sNDA for upadacitinib in the treatment of adult patients with active psoriatic arthritis.
The FDA has extended the updated Prescription Drug User Fee Act (PDUFA) action date by three months to late the second-quarter of 2021.
AbbVie recently received an information request from the FDA for an updated assessment of the benefit-risk profile for upadacitinib in psoriatic arthritis. AbbVie responded to the request and the FDA will require additional time for a full review of the submission.
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NORTH CHICAGO, Ill., March 17, 2021 /PRNewswire/ AbbVie (NYSE:ABBV), a global research and development-based biopharmaceutical company, announced that the U.S. Food and Drug Administration (FDA) has extended the review period for the supplemental New Drug Application (sNDA) for upadacitinib in the treatment of adult patients with active psoriatic arthritis. The updated Prescription Drug User Fee Act (PDUFA) action date has been extended three months to late Q2 2021.
AbbVie recently received an information request from the FDA for an updated assessment of the benefit-risk profile for upadacitinib in psoriatic arthritis. AbbVie responded to the request and the FDA will require additional time for a full review of the submission.
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Merck Receives Priority Review From FDA for New Drug Application for HIF-2? Inhibitor Belzutifan
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