Leqselvi — CareFirst (Caremark)
Severe alopecia areata
Preferred products
- Litfulo
 - Olumiant
 
Initial criteria
- Age ≥ 18 years (adult member)
 - Prescribed by or in consultation with a dermatologist
 - 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 (which can include a tuberculosis skin test [TST] or an interferon-release assay [IGRA]) within 12 months of initiating therapy for persons naïve to biologic drugs or targeted synthetic drugs associated with increased TB risk
 - If TB screening test is positive, further testing confirms no active disease (e.g., chest x-ray)
 - Do not administer medication in members with active TB infection; if latent disease, TB treatment must start before initiation
 - Medication is not used concomitantly with any other biologic drug, targeted synthetic drug, or potent immunosuppressant such as azathioprine or cyclosporine
 - Authorization may alternatively be granted for adult members who have previously received a targeted synthetic drug (e.g., Litfulo, Olumiant) indicated for treatment of severe alopecia areata in the past year
 
Reauthorization criteria
- Adult member using the medication for severe alopecia areata
 - 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])
 - Continued absence of active TB infection and adherence to TB management requirements
 - Medication is not used concomitantly with any other biologic drug, targeted synthetic drug, or potent immunosuppressant such as azathioprine or cyclosporine
 
Approval duration
12 months