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LeqselviCareFirst (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