Risankizumab (Skyrizi)

CDA-AMC

doi:10.51731/cjht.2026.1430

Vol. 6 No. 4 (2026): April

Reimbursement Reviews

Risankizumab (Skyrizi)

CDA-AMC

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DOI: https://doi.org/10.51731/cjht.2026.1430

Published April 30, 2026

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Key Messages

Reimbursement reviews are comprehensive assessments of the clinical effectiveness and cost-effectiveness, as well as patient and clinician perspectives, of a drug or drug class.
The assessments inform nonbinding recommendations that help guide the reimbursement decisions of Canada’s federal, provincial, and territorial governments, with the exception of Quebec.
This review assesses Skyrizi (Risankizumab): 600 mg in 10 mL (60 mg/mL) by IV infusion; 180 mg in 1.2 mL (150 mg/mL) by subcutaneous injection; 360 mg in 2.4 mL (150 mg/mL) by subcutaneous injection.
Indication: For the treatment of adult patients with moderately to severely active UC who have had an inadequate response, loss of response, or were intolerant to conventional therapy, a biologic treatment, or a JAK inhibitor.

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