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    • This website is for UK Healthcare Professionals only

      Expert Perspectives


      SKYRIZI vs secukinumab5

      Efficacy of SKYRIZI


      PASI 100: SKYRIZI vs. Ustekinumab2

      PASI 90: SKYRIZI vs. Ustekinumab2

      Efficacy - SKYRIZI vs. adalimumab4

      2 year SKYRIZI efficacy data from IMMhance3

      2.5 year efficacy and safety data from UltIMMa OLE study10


      Dr Kave Shams discusses the benefits of 12 weekly maintenance dosing offered with SKYRIZI

      Safety Profile1,2,3,4

      Dr Savage discusses the Safety Profile of SKYRIZI from the Phase III studies


      Dr Kave Shams discusses the mode of action of SKYRIZI and the IL-23/Th17 pathway

      SKYRIZI mode of action animation


      1. SKYRIZI: Summary of Product Characteristics 2020.
      2. Gordon KB et al. Lancet 2018;392: 650-661.
      3. IMMhance. Blauvelt A et al. Poster presented WCD June 2019 P478.
      4. IMMvent. Reich K et al. Lancet 2019;394: 576-586.
      5. Warren RB et al. Risankizumab vs Secukinumab in Patients with Moderate-to-Severe Plaque Psoriasis: A Phase 3 Trial, Presented at AAD 2020.
      6. Gooderham MJ et al. J Eur Acad Dermatol Venereol 2018; 32(7):1111-1119.
      7. Kofoed K et al. Acta Derm Venereol. 2015;95(2):133-139.
      8. Gaffen SL et al. Nat Rev Immunol 2014; 14(9): 585-600.
      9. Girolomoni G et al. J Eur Acad Dermatol Venereol 2017; 31(1): 1616-1626.
      10. Lynde CW et al. J Am Acad Dermatol 2014; 71(1): 141-150.
      11. UltIMMa open label extension study. Bachelez H et al. EADV Oct 2019. P1764.

      UK-RISN-210078. Date of preparation: February 2021. 

      SKYRIZI™  (risankizumab) is indicated for the treatment of moderate to severe plaque psoriasis in adults who are candidates for systemic therapy.1
      The recommended dose of SKYRIZI is 150mg (two 75mg injections) administered by subcutaneous injection at Week 0, Week 4, and every 12 weeks thereafter.
      SKYRIZI is intended for use under the guidance and supervision of a physician experienced in the diagnosis and treatment of psoriasis.
      Some patients may not be suitable for SKYRIZI. You are advised to read the Prescribing Information (which can be found on tab above). Please also refer to the SKYRIZI Summary of Product Characteristics for important information including special warnings/precautions for use and summary of adverse reactions.
      Study design information can be found on the Study Design page.

      Adverse events should be reported. Reporting forms and information can be found at yellowcard.mhra.gov.uk.
      Adverse events should also be reported to AbbVie on GBPV@abbvie.com