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adalimumab-bwwdCareFirst (Caremark)

Immune checkpoint inhibitor-related inflammatory arthritis

Initial criteria

  • Member age ≥ 2 years (for uveitis)
  • Requested medication is used for an indication outlined in the coverage criteria section
  • Member has a documented negative tuberculosis (TB) test within 12 months of initiating therapy for persons naïve to biologic or targeted synthetic drugs associated with increased TB risk
  • If TB screening is positive, further testing confirms no active disease (e.g., chest x-ray)
  • Do not administer requested medication to members with active TB infection
  • If latent TB disease is present, TB treatment must be started before initiation of requested medication
  • Member is not using the requested medication concomitantly with any other biologic drug or targeted synthetic drug for the same indication
  • For rheumatoid arthritis: member must initiate treatment with every other week dosing

Reauthorization criteria

  • Uveitis: Member continues to achieve or maintain a positive clinical response as evidenced by low disease activity or improvement in signs and symptoms, meeting any of the following:
  • • Reduced frequency of disease flares compared to baseline
  • • Stability or improvement in anterior chamber (AC) cell grade compared to baseline
  • • Stability or improvement in vitreous haze (VH) grade compared to baseline
  • • Stability or improvement in visual acuity compared to baseline
  • • Reduction in glucocorticoid requirements from baseline
  • • No new active inflammatory chorioretinal and/or inflammatory retinal vascular lesions relative to baseline
  • Immune checkpoint inhibitor-related inflammatory arthritis: Member achieves or maintains a positive clinical response as evidenced by low disease activity or improvement in signs and symptoms
  • All other covered indications: Member achieves or maintains a positive clinical response as evidenced by low disease activity or improvement in signs and symptoms

Approval duration

12 months