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Otezla (apremilast)Blue Cross Blue Shield of Texas

FDA labeled indications

Initial criteria

  • Patient has diagnosis meeting an FDA labeled indication OR a compendia supported indication (AHFS, DrugDex 1, 2a, or 2b, NCCN 1, 2a, or 2b recommended use)
  • If indication is Behçet’s disease, patient tried, intolerant, contraindicated, or had inadequate response to one conventional agent (e.g., azathioprine) OR use of another biologic immunomodulator FDA labeled for BD
  • Patient’s age is within FDA labeling for the requested indication OR agent use supported for patient’s age OR agent has compendia supported indication for patient’s age
  • Patient will NOT be using the requested agent with another immunomodulatory agent (e.g., TNF inhibitors, JAK inhibitors, IL-4 inhibitors) OR if combination, BOTH of: prescribing information does not limit combination use AND support (clinical trial, phase III study, or guideline) provided
  • ONE of: patient has mild severity plaque psoriasis OR prescriber is a specialist in patient's diagnosis area or has consulted with a specialist
  • Patient does NOT have any FDA labeled contraindications to the requested agent

Reauthorization criteria

  • Patient was previously approved for requested agent through plan’s prior authorization process
  • Patient has had clinical benefit with requested agent
  • Patient will NOT be using with another immunomodulatory agent OR if combination, BOTH: prescribing information does not limit combination AND support for combination therapy provided
  • ONE of: patient has mild severity plaque psoriasis OR prescriber is a specialist or has consulted a specialist
  • Patient does NOT have any FDA labeled contraindications to requested agent

Approval duration

12 months