Olumiant — CareFirst (Caremark)
severe alopecia areata
Initial criteria
- age ≥ 18 years
- Member has previously received a targeted synthetic drug (e.g., Leqselvi, Litfulo) indicated for treatment of severe alopecia areata in the past year OR meets both of the following:
- • Member has at least 50% scalp hair loss (e.g., Severity of Alopecia Tool [SALT] score ≥ 50)
- • Other forms of alopecia have been ruled out (e.g., androgenetic alopecia, trichotillomania, telogen effluvium, chemotherapy-induced hair loss, tinea capitis)
- Member has had 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
- If TB screening is positive, active disease must be ruled out (e.g., chest x-ray); members with active TB infection must not receive therapy; latent disease must be treated before initiation
- Medication is not used concomitantly with any other biologic drug, targeted synthetic drug, or potent immunosuppressant such as azathioprine or cyclosporine
- Prescribed by or in consultation with a dermatologist
Reauthorization criteria
- Member achieves or maintains a positive clinical response as evidenced by improvement in signs and symptoms from baseline (e.g., increased scalp hair coverage, 80% total scalp hair coverage [SALT score ≤ 20])
Approval duration
12 months