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Arcalyst (rilonacept subcutaneous injection)Cigna

Deficiency of Interleukin-1 Receptor Antagonist (DIRA)

Initial criteria

  • Patient is ≥ 10 kg (22 pounds); AND
  • Genetic testing has confirmed bi-allelic pathogenic variants in the IL1RN gene; AND
  • According to the prescriber, patient has demonstrated a clinical benefit with Kineret (anakinra subcutaneous injection); AND
  • The medication is prescribed by or in consultation with a rheumatologist, geneticist, dermatologist, or a physician specializing in the treatment of autoinflammatory disorders

Reauthorization criteria

  • Patient has been established on this medication for at least 6 months; AND
  • Patient meets at least ONE of the following: (a) When assessed by at least one objective measure, patient experienced a beneficial clinical response from baseline (prior to initiating the requested drug); OR (b) Compared with baseline, patient experienced an improvement in at least one symptom

Approval duration

initial 6 months; reauth 1 year