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Tryngolza (olezarsen)Blue Cross Blue Shield of Oklahoma

other FDA labeled indications

Initial criteria

  • ONE of the following: (A) Diagnosis of familial chylomicronemia syndrome (FCS) confirmed by (1) genetic confirmation of bi-allelic pathogenic variants in affected genes (e.g., LPL, ApoA5, ApoC2, LMF1, GPIHBP1, G3PDH1) OR (2) ALL of the following: (A) Fasting triglyceride (TG) levels >880 mg/dL for 3 consecutive measurements AND (B) Secondary causes of hypertriglyceridemia ruled out AND (C) History of pancreatitis or unexplained recurrent abdominal pain AND (D) No response (TG decrease <20%) to conventional lipid lowering therapies (fibrates, omega-3 fatty acids, statins, niacin, ezetimibe, PCSK9 inhibitors) OR (B) Another FDA labeled indication for the agent and route OR (C) Another compendia-supported indication for the agent and route
  • If patient has an FDA labeled indication: ONE of the following: (A) Patient’s age is within FDA labeling OR (B) There is support for use at the patient’s age
  • Prescriber is a specialist (cardiologist, endocrinologist, geneticist, lipidologist) or has consulted with a specialist
  • Patient has no FDA labeled contraindications to the requested agent

Reauthorization criteria

  • Patient was previously approved for the requested agent through the plan’s Prior Authorization process
  • Patient has had clinical benefit with the requested agent
  • Prescriber is a specialist (cardiologist, endocrinologist, geneticist, lipidologist) or has consulted with a specialist
  • Patient has no FDA labeled contraindications to the requested agent

Approval duration

12 months