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CystaranCareFirst (Caremark)

treatment of corneal cystine crystal accumulation in patients with cystinosis

Initial criteria

  • Diagnosis of cystinosis confirmed by the presence of increased cystine concentration in leukocytes or by genetic testing
  • Member has corneal cystine crystal accumulation
  • Medication prescribed by or in consultation with an ophthalmologist or a physician who specializes in the treatment of metabolic disease and/or lysosomal storage disorders

Reauthorization criteria

  • Member is responding to therapy as evidenced by either of the following:
  • • Member has experienced a decrease in corneal cystine crystal accumulation
  • • Member did not experience an increase in corneal cystine crystal accumulation

Approval duration

12 months