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The Policy VaultThe Policy Vault

NexlizetBlue Cross Blue Shield of Alabama

Reducing the risk of myocardial infarction and coronary revascularization in adults with high risk for cardiovascular disease (CVD) event or established CVD (acute coronary syndrome, history of myocardial infarction, stable or unstable angina, coronary or other arterial revascularization, stroke, transient ischemic attack, or peripheral arterial disease including aortic aneurysm presumed to be of atherosclerotic origin)

Initial criteria

  • ONE of the following: • Diagnosis of primary hyperlipidemia (including heterozygous familial hypercholesterolemia [HeFH]) OR • For reducing the risk of myocardial infarction and coronary revascularization and ONE of: – High risk for a cardiovascular disease (CVD) event OR – Established CVD with: ▪ Acute coronary syndrome ▪ History of myocardial infarction ▪ Stable or unstable angina ▪ Coronary or other arterial revascularization ▪ Stroke ▪ Transient ischemic attack ▪ Peripheral arterial disease, including aortic aneurysm presumed to be of atherosclerotic origin
  • AND ONE of the following: • Tried and had inadequate response to at least one statin OR • Statin intolerant defined as experiencing ONE of: – Statin-related rhabdomyolysis – Statin-related skeletal muscle symptoms (e.g., myopathy, myalgia) – Statin-related elevated hepatic transaminase – Hypersensitivity to at least one statin – FDA labeled contraindication to all statins
  • OR • Another FDA labeled or compendia-supported indication exists for the requested agent and route of administration (AHFS or DrugDex 1 or 2a level of evidence)
  • AND ONE of the following: • Patient age is within FDA labeling for the requested indication OR • There is support for using the agent for patient’s age
  • AND • Patient does not have any FDA labeled contraindications to the requested agent

Reauthorization criteria

  • • Patient has been previously approved for the requested agent through the plan’s Prior Authorization process • Patient has had clinical benefit with the requested agent • Patient does not have any FDA labeled contraindications to the requested agent • Compendia allowed: AHFS or DrugDex 1 or 2a level of evidence

Approval duration

12 months