Cosentyx (secukinumab) Sensoready pen — United Healthcare
Plaque Psoriasis
Initial criteria
- Diagnosis of moderate to severe plaque psoriasis
- One of the following: (a) All of the following: i. ≥3% body surface area involvement, palmoplantar, facial, genital involvement, or severe scalp psoriasis AND ii. History of failure to one topical therapy (corticosteroids, vitamin D analogs, tazarotene, calcineurin inhibitors, anthralin, coal tar), unless contraindicated or adverse effects AND iii. History of failure to a 3-month trial of methotrexate at maximally indicated dose, unless contraindicated or adverse effects OR (b) Previously treated with a targeted immunomodulator FDA-approved for plaque psoriasis (e.g., Cimzia, adalimumab, Otezla, Skyrizi, Stelara, Tremfya, Enbrel) OR (c) Currently on Cosentyx therapy with documentation and has not received manufacturer supplied sample or assistance
- Patient is not receiving Cosentyx in combination with another targeted immunomodulator [e.g., Enbrel, Cimzia, Simponi, Orencia, adalimumab, Stelara, Skyrizi, Tremfya, Taltz, Siliq, Ilumya, Xeljanz, Olumiant, Rinvoq, Otezla]
- Prescribed by or in consultation with a dermatologist
Reauthorization criteria
- Documentation of positive clinical response to Cosentyx therapy
- Not receiving Cosentyx in combination with another targeted immunomodulator [Enbrel, Cimzia, Simponi, Orencia, adalimumab, Stelara, Skyrizi, Tremfya, Taltz, Siliq, Ilumya, Xeljanz, Olumiant, Rinvoq, Otezla]
Approval duration
12 months