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AbbVie’s Skyrizi (risankizumab-rzaa) Receives the US FDA’s Approval for the Treatment of Active Psoriatic Arthritis

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AbbVie’s Skyrizi (risankizumab-rzaa) Receives the US FDA’s Approval for the Treatment of Active Psoriatic Arthritis

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  • The approval is based on the 2 (KEEPsAKE-1 /2) studies evaluating Skyrizi (150mg, SC) vs PBO in adults with active PsA who had responded inadequately or were intolerant to biologic therapy & non-biologic DMARDs
  • The trial met the 1EPs i.e., @24wks., patients achieved the ACR20 response (57.3% & 51.3% vs 33.5% & 26.5%), improvements in ACR50, ACR70 responses, physical function, joint symptoms, improvements in other manifestations of PsA including dactylitis & enthesitis, skin lesions of psoriasis & the safety profile was consistent with patients with PsO
  • Skyrizi is an IL-23 inhibitor that blocks IL-23 by binding to its p19 subunit while P-III trials in psoriasis, CD, UC & PsA are ongoing

Ref: AbbVie | Image: abbvie

Click here to­ read the full press release 

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