Adalimumab-aacf — Blue Cross Blue Shield of Illinois
psoriatic arthritis
Preferred products
- Adalimumab-aaty
- Adalimumab-adbm
- Adalimumab-ryvk
- Amjevita (adalimumab-atto)
- Cyltezo (adalimumab-adbm)
- 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 Abrilada, Adalimumab-ryvk, Amjevita, Cyltezo (adalimumab-adbm), Hulio (adalimumab-fkjp), Humira, Hyrimoz, Idacio (adalimumab-aacf), Yuflyma, Yusimry are eligible for continuation; OR (B) ALL of the following:
- – The patient has an FDA labeled or compendia-supported indication for the requested agent and route of administration AND
- Diagnosis of moderately to severely active rheumatoid arthritis AND ONE of the following:
- • Tried and had inadequate response to maximally tolerated methotrexate (up to 25 mg weekly) for ≥3 months OR
- • Tried and had inadequate response to ONE conventional agent (hydroxychloroquine, leflunomide, sulfasalazine) for ≥3 months OR
- • Intolerance or hypersensitivity to ONE conventional agent (methotrexate, hydroxychloroquine, leflunomide, sulfasalazine) OR
- • FDA labeled contraindication to ALL conventional agents (methotrexate, hydroxychloroquine, leflunomide, sulfasalazine) OR
- • Medication history indicates use of another biologic immunomodulator FDA labeled or compendia-supported for RA
- OR Diagnosis of active psoriatic arthritis AND ONE of the following:
- • Tried and had inadequate response to ONE conventional agent (cyclosporine, leflunomide, methotrexate, sulfasalazine) for ≥3 months OR
- • Intolerance or hypersensitivity to ONE conventional agent used for PsA OR
- • FDA labeled contraindication to ALL conventional agents used for PsA OR
- • Severe active PsA (e.g., erosive disease, elevated markers, long-term functional damage, rapidly progressive) OR
- • Concomitant severe psoriasis (greater than 10% BSA, or on sensitive sites, or serious emotional/pruritic impact) OR
- • Medication history indicates use of another biologic immunomodulator agent or Otezla for PsA