FDA Approved Indications:
Treatment of advanced renal cell carcinoma after treatment failure with sunitinib or sorafenib.
All FDA-approved indications not otherwise excluded from Part D.
NA
Must be prescribed by an oncologist.
For initiation of treatment, a prior authorization form and relevant chart notes documenting medical rationale are required and for continuation of therapy, ongoing documentation of successful response to the medication may be necessary.
Patient must have a diagnosis of advanced renal cell carcinoma and have had disease progression on sunitinib, sorafenib or both.
NA
Initial prior authorization and reauthorization will be approved for up to six months.