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anakinraCareFirst (Caremark)

Moderately to severely active rheumatoid arthritis (RA)

Initial criteria

  • Age ≥ 18 years
  • Member meets either of the following biomarker criteria: (a) Positive for rheumatoid factor (RF) or anti-cyclic citrullinated peptide (anti-CCP); OR (b) Tested for RF, anti-CCP, and C-reactive protein (CRP) and/or erythrocyte sedimentation rate (ESR)
  • Member meets ONE of the following regarding methotrexate (MTX) and conventional synthetic DMARDs:
  • 1. Failed to achieve low disease activity after 3-month trial of MTX monotherapy (≥15 mg/week) and had inadequate response or intolerance to, or contraindication to hydroxychloroquine and/or sulfasalazine; and has moderate to high disease activity
  • 2. Unable to tolerate 3-month trial of MTX monotherapy and had inadequate response or intolerance to, or contraindication to leflunomide, hydroxychloroquine, or sulfasalazine; and has moderate to high disease activity
  • 3. Experienced intolerable adverse event or contraindication to MTX, discontinued MTX, and had inadequate response or intolerance to, or contraindication to leflunomide, hydroxychloroquine, or sulfasalazine; and has moderate to high disease activity

Reauthorization criteria

  • Documentation supporting positive clinical response

Approval duration

12 months