Bimzelx (bimekizumab-bkzx) — United Healthcare
Plaque Psoriasis (PsO)
Preferred products
- preferred adalimumab products
- Cimzia (certolizumab)
- Cosentyx (secukinumab)
- Enbrel (etanercept)
- Skyrizi (risankizumab)
- Sotyktu (deucravacitinib)
- preferred ustekinumab products
- Tremfya (guselkumab)
Initial criteria
- Diagnosis of moderate to severe plaque psoriasis
- AND one of the following:
- (a) All of the following: i. ≥3% body surface area involvement OR palmoplantar/facial/genital involvement OR severe scalp psoriasis AND ii. History of failure to one topical therapy unless contraindicated or clinically significant adverse effects (document drug, date, and duration of trial): corticosteroids, vitamin D analogs, tazarotene, calcineurin inhibitors, anthralin, or coal tar AND iii. History of failure to a 3-month trial of methotrexate at maximum indicated dose unless contraindicated or clinically significant adverse effects
- OR (b) Patient previously treated with a targeted immunomodulator FDA-approved for plaque psoriasis (document drug, date, and duration of therapy)
- AND one of the following: (a) History of failure, contraindication, or intolerance to two of: preferred adalimumab product, Cimzia, Cosentyx, Enbrel, Skyrizi, Sotyktu, preferred ustekinumab product, or Tremfya OR (b) Both: (i) Currently on Bimzelx therapy as documented AND (ii) Has not received manufacturer sample or UCB assistance to establish current use
- AND Patient not receiving Bimzelx in combination with another targeted immunomodulator (list provided)
- AND Prescribed by or in consultation with a dermatologist
Reauthorization criteria
- Documentation of positive clinical response to Bimzelx therapy
- AND patient is not receiving Bimzelx in combination with another targeted immunomodulator (list provided)
Approval duration
12 months