Revuforj (revumenib)

Indications for Prior Authorization

Revuforj (revumenib)
  • 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

2025-04-14, 2024-12-24

  1. Revuforj Prescribing Information. Syndax Pharmaceuticals, Inc. November 2024

  • 2025-04-14: Added Revuforj 25mg to guideline
  • 2024-12-24: New Program.

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