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Bimzelx (bimekizumab-bkzx)CareFirst (Caremark)

moderate to severe plaque psoriasis (PsO)

Initial criteria

  • Member is an adult (age ≥ 18 years) with moderate to severe plaque psoriasis.
  • Authorization of 12 months may be granted for members who have previously received a biologic or targeted synthetic drug (e.g., Sotyktu, Otezla) indicated for treatment of moderate to severe plaque psoriasis.
  • Authorization of 12 months may be granted when any of the following criteria is met:
  • • Crucial body areas (e.g., hands, feet, face, neck, scalp, genitals/groin, intertriginous areas) are affected.
  • • At least 10% of body surface area (BSA) is affected.
  • • At least 3% of BSA is affected AND member has had an inadequate response or intolerance to either phototherapy (e.g., UVB, PUVA) or pharmacologic treatment with methotrexate, cyclosporine, or acitretin, OR has a clinical reason to avoid those therapies.
  • Member has a documented negative tuberculosis (TB) test within 12 months of initiating therapy if naïve to biologic or targeted synthetic drugs associated with increased TB risk.
  • Member cannot use Bimzelx concomitantly with any other biologic drug or targeted synthetic drug for the same indication.

Reauthorization criteria

  • Adult member who is using Bimzelx for moderate to severe plaque psoriasis shows positive clinical response evidenced by low disease activity or improvement in signs/symptoms when either:
  • • Reduction in 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