Revuforj (revumenib)
Indications for Prior Authorization
Revuforj (revumenib)
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For diagnosis of Relapsed or Refractory Acute Leukemia
Indicated for the treatment of relapsed or refractory acute leukemia with a lysine methyltransferase 2A gene (KMT2A) translocation in adult and pediatric patients 1 year and older.
Criteria
Revuforj
Prior Authorization (Initial Authorization)
Length of Approval: 12 Month(s)
- Diagnosis of acute leukemia AND
- Disease is relapsed or refractory AND
- Patient is 1 year of age or older AND
- Presence of lysine methyltransferase 2A gene (KMT2A) translocation
Revuforj
Prior Authorization (Reauthorization)
Length of Approval: 12 Month(s)
- Patient does not show evidence of progressive disease while on therapy
P & T Revisions
2024-12-24
References
- Revuforj Prescribing Information. Syndax Pharmaceuticals, Inc. November 2024
Revision History
- 2024-12-24: New Program.