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AetnaCommercial · Prior Auth · Medical Policy · Dermatology, Rheumatology, GastroenterologyMedium impact

Risankizumab-rzaa (Skyrizi) (CPB 1009, reviewed 2026-10-14)

Effective date
Not stated in the notice
Identified
Oct 19, 2026

Summary

Aetna's Clinical Policy Bulletin 1009 covers risankizumab-rzaa (Skyrizi) for commercial medical plans, and precertification is required of all Aetna participating providers and members in applicable plan designs for intravenous risankizumab-rzaa. Aetna considers it medically necessary for moderate to severe plaque psoriasis in members 6 years of age or older who have previously received a biologic or targeted synthetic drug, or when crucial body areas, at least 10% of body surface area, or at least 3% of body surface area with an inadequate response or intolerance to phototherapy or methotrexate, cyclosporine, or acitretin is affected. It also covers active psoriatic arthritis, moderately to severely active Crohn's disease, and moderately to severely active ulcerative colitis, and Aetna considers concomitant use with another biologic or targeted synthetic drug for the same indication experimental, investigational, or unproven.

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What to do

Action · 5 steps
01Already effective 07/14/2022: Billing team: obtain precertification for intravenous risankizumab-rzaa (HCPCS J2327) by calling (866) 752-7021 or faxing (888) 267-3277.
02The medication must be prescribed by or in consultation with a dermatologist for plaque psoriasis, a rheumatologist or dermatologist for psoriatic arthritis, or a gastroenterologist for Crohn's disease and ulcerative colitis.
03Document that the member has been evaluated for tuberculosis infection before starting treatment, and document that the member is not using the requested medication concomitantly with another biologic or targeted synthetic drug for the same indication.
04For continuation, document the response from baseline that the policy lists for each condition, such as reduced body surface area affected or improved signs and symptoms for plaque psoriasis, or improved swollen or tender joint counts, dactylitis, enthesitis, skin or nail involvement, functional status, or CRP for psoriatic arthritis.
05Crohn's disease induction is 600 mg intravenously at Week 0, Week 4, and Week 8, and ulcerative colitis induction is 1200 mg intravenously at Week 0, Week 4, and Week 8.

Codes mentioned

J2327L40.0

Original notice

Risankizumab-rzaa (Skyrizi) (CPB 1009, reviewed 2026-10-14)
aetna.com · Always check the source before changing claims.
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