ozanimod — Blue Cross Blue Shield of Illinois
other FDA labeled indications
Initial criteria
- Member resides in Ohio
- Plan is Fully Insured or HIM Shop (SG)
- Patient does NOT have any FDA labeled contraindications to the requested agent
- ONE of the following: (a) Patient has another FDA labeled indication for the requested agent and route of administration OR (b) Patient has an indication supported in compendia for the requested agent and route of administration OR (c) Prescriber has submitted TWO peer-reviewed journal articles supporting the proposed use as generally safe and effective
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
- Prescriber is a specialist in the area of the patient’s diagnosis or has consulted with one
- For multiple sclerosis: ONE of the following: (a) Patient will NOT use the requested agent with another disease modifying agent (DMA) OR (b) Patient will use the requested agent in combination with Mavenclad (cladribine) AND there is clinical support for this use (e.g., relapse between cycles of Mavenclad)
- For ulcerative colitis: ONE of the following: (a) Patient will NOT use the requested agent in combination with immunomodulatory agents (e.g., TNF inhibitors, JAK inhibitors, IL-4 inhibitors) OR (b) The requested agent’s prescribing information does NOT limit use with another immunomodulatory agent AND there is support for combination therapy (e.g., guidelines, clinical trials)
- Patient does NOT have any FDA labeled contraindications to the requested agent
Approval duration
12 months