Otezla (apremilast) — Blue Cross Blue Shield of Texas
compendia supported 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