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