Ojjaara (momelotinib) - PA, NF

Indications for Prior Authorization

Ojjaara (momelotinib)
  • For diagnosis of Myelofibrosis
    Indicated for the treatment of intermediate or high risk myelofibrosis (MF), including primary MF or secondary MF [post-polycythemia vera (PV) and post-essential thrombocythemia (ET)], in adults with anemia.

Criteria

Ojjaara

Prior Authorization (Initial Authorization)

Length of Approval: 6 Month(s)
For diagnosis of Myelofibrosis

  • Diagnosis of one of the following:
    • Primary myelofibrosis
    • Post-polycythemia vera myelofibrosis
    • Post-essential thrombocythemia myelofibrosis
    AND
  • Disease is intermediate or high risk
  • AND
  • Patient has anemia
  • AND
  • One of the following:
    • Both of the following:
      • Platelet count is greater than or equal to 50 x 10^9/L
      • AND
      • One of the following:
        • Trial and failure, contraindication, or intolerance to Jakafi (ruxolitinib)
        • OR
        • For continuation of prior therapy
      OR
    • Platelet count is less than 50 x 10^9/L
Ojjaara

Prior Authorization (Reauthorization)

Length of Approval: 12 Month(s)
For diagnosis of Myelofibrosis

  • Documentation of positive clinical response to therapy (e.g., symptom improvement, spleen volume reduction)
Ojjaara

Non Formulary

Length of Approval: 6 Month(s)
For diagnosis of Myelofibrosis

  • Submission of medical records (e.g., chart notes) confirming a diagnosis of one of the following:
    • Primary myelofibrosis
    • Post-polycythemia vera myelofibrosis
    • Post-essential thrombocythemia myelofibrosis
    AND
  • Disease is intermediate or high risk
  • AND
  • Patient has anemia
  • AND
  • One of the following:
    • Both of the following:
      • Submission of medical records (e.g., chart notes) confirming the platelet count is greater than or equal to 50 x 10^9/L
      • AND
      • One of the following:
        • Paid claims or submission of medical records (e.g., chart notes) confirming trial and failure, contraindication, or intolerance to Jakafi (ruxolitinib)
        • OR
        • For continuation of prior therapy
      OR
    • Submission of medical records (e.g., chart notes) confirming the platelet count is less than 50 x 10^9/L
P & T Revisions

2024-11-05, 2024-03-05

  1. Ojjaara Prescribing Information. GlaxoSmithKline. Durham, NC. September 2023.

  • 2024-11-05: Annual Review. No updates
  • 2024-03-05: Addition of a step through Jakafi and NF criteria

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