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brodalumabCareFirst (Caremark)

moderate to severe plaque psoriasis (PsO)

Initial criteria

  • Age ≥ 18 years
  • Medication is prescribed by or in consultation with a dermatologist
  • Member has a documented negative tuberculosis (TB) test within 12 months prior to initiating therapy if naïve to biologic or targeted synthetic drugs; if positive, further testing shows no active disease and latent disease is treated before starting therapy
  • Member is not using the requested medication concomitantly with any other biologic drug or targeted synthetic drug for the same indication
  • Authorization of 12 months may be granted for adult members who have previously received a biologic or targeted synthetic drug (e.g., Sotyktu, Otezla) indicated for moderate to severe plaque psoriasis OR when any of the following are met:
  • • Crucial body areas (hands, feet, face, neck, scalp, genitals/groin, intertriginous areas) are affected
  • • ≥10% of body surface area (BSA) is affected
  • • ≥3% of BSA is affected AND one of the following: (a) inadequate response or intolerance to phototherapy (UVB, PUVA) or systemic pharmacologic treatment with methotrexate, cyclosporine, or acitretin; OR (b) clinical reason to avoid methotrexate, cyclosporine, and acitretin

Reauthorization criteria

  • Member is an adult using the medication for moderate to severe plaque psoriasis
  • Member has achieved or maintained a positive clinical response as evidenced by either:
  • • Reduction in body surface area (BSA) affected from baseline OR
  • • Improvement in signs and symptoms from baseline (e.g., itching, redness, flaking, scaling, burning, cracking, pain)

Approval duration

12 months