Adalimumab-aacf — Blue Cross Blue Shield of Illinois
moderate to severe plaque psoriasis (PS)
Preferred products
- Adalimumab
- Adalimumab-aaty
- Humira (adalimumab)
- Hadlima (adalimumab-bwwd)
- Simlandi (adalimumab-ryvk)
Initial criteria
- ONE of the following: A. The requested agent is eligible for continuation of therapy AND ONE of the following: Agents Eligible for Continuation of Therapy - All target agents EXCEPT specified are eligible for continuation
- If the requested agent is NOT a preferred agent, prescriber states patient has been treated with the requested agent (not samples) within past 90 days AND is at risk if therapy is changed
- If the requested agent is a preferred agent, prescriber states patient has been treated with the requested agent (not samples) within past 90 days AND is at risk if therapy is changed
- OR B. ALL of the following: patient has FDA labeled indication or compendia supported indication for requested agent and route AND ONE of the following indication-specific criteria:
- For rheumatoid arthritis (RA): patient has tried and had inadequate response to methotrexate ≥3 months OR inadequate response to one conventional agent (hydroxychloroquine, leflunomide, sulfasalazine) ≥3 months OR intolerance/hypersensitivity to one conventional agent OR contraindication to all conventional agents OR medication history of another biologic immunomodulator for RA
- For psoriatic arthritis (PsA): patient has tried and had inadequate response to one conventional agent (cyclosporine, leflunomide, methotrexate, sulfasalazine) ≥3 months OR intolerance/hypersensitivity to one conventional agent OR contraindication to all conventional agents OR severe active PS features (≥10% BSA or sensitive areas or intractable pruritus/emotional consequences) OR severe active PsA (erosive, elevated inflammation markers, long-term functional damage, rapidly progressive) OR medication history of another biologic immunomodulator or Otezla for PsA
- For plaque psoriasis (PS): patient has tried and had inadequate response to one conventional agent (acitretin, anthralin, calcipotriene, calcitriol, coal tar products, cyclosporine, methotrexate, pimecrolimus, PUVA, tacrolimus, tazarotene, topical corticosteroids) ≥3 months