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