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Cerdelga (eliglustat)CareFirst (Caremark)

Gaucher disease type 1

Initial criteria

  • Member is age ≥ 18 years.
  • Diagnosis of Gaucher disease is confirmed by enzyme assay demonstrating a deficiency of beta-glucocerebrosidase (glucosidase) enzyme activity or by genetic testing.
  • Member is a CYP2D6 extensive metabolizer, intermediate metabolizer, or poor metabolizer as detected by an FDA‑cleared test.

Reauthorization criteria

  • Member meets the criteria for initial approval.
  • Member is not experiencing an inadequate response or any intolerable adverse events from therapy.

Approval duration

12 months