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NityrCigna

Hereditary Tyrosinemia Type 1

Initial criteria

  • Diagnosis is supported by ONE of the following (i or ii): i. Genetic testing confirms biallelic pathogenic or likely pathogenic variants in the FAH gene; OR ii. Patient has elevated levels of succinylacetone in the serum or urine; AND
  • Medication is prescribed in conjunction with a tyrosine- and phenylalanine-restricted diet; AND
  • Patient will not be taking the requested agent concurrently with another nitisinone product; AND
  • Medication is prescribed by or in consultation with a metabolic disease specialist (or specialist who focuses in the treatment of metabolic diseases)

Approval duration

1 year