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AbbVie Seeks EMA Approval for Subcutaneous Skyrizi in Crohn’s Disease

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Sig2.55Sen+4.14Env0.00Soc+2.25Gov+0.53

AbbVie submitted a regulatory application to the European Medicines Agency seeking approval for subcutaneous (SC) induction of Skyrizi (risankizumab) in adults with moderately to severely active Crohn’s disease. If approved, SC induction would add to the current IV induction, followed by SC maintenance every eight weeks, aiming for greater convenience and competitive positioning despite pricing headwinds and rising competitive pressure.

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