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Procysbi (cysteamine bitartrate)Blue Cross Blue Shield of Alabama

Nephropathic cystinosis

Preferred products

  • Cystagon (immediate-release cysteamine)

Initial criteria

  • ONE of the following:
  • - The patient has a diagnosis of nephropathic cystinosis OR
  • - The patient has another FDA labeled indication for the requested agent and route of administration OR
  • - The patient has an indication that is supported in compendia for the requested agent and route of administration
  • AND if the patient has an FDA labeled indication, then ONE of the following:
  • - The patient’s age is within FDA labeling for the requested indication OR
  • - There is support for using the requested agent for the patient’s age for the requested indication
  • AND ONE of the following:
  • - The patient has tried and had an inadequate response to Cystagon (immediate-release cysteamine) OR
  • - The patient has an intolerance or hypersensitivity to Cystagon that is not expected to occur with the requested agent OR
  • - The patient has an FDA labeled contraindication to Cystagon that is not expected to occur with the requested agent
  • AND The prescriber is a specialist in the area of the patient’s diagnosis (e.g., nephrologist) or has consulted with such a specialist
  • AND The patient does NOT have any FDA-labeled contraindications to the requested agent

Approval duration

12 months