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

Happy New Year! If you are calling our Member Services department today, we ask for your patience while our entire team assists members with their questions. The first week in January is always the busiest time of year and we will get to your call as soon as possible. Members may find the information you need by logging into our secure MyWHA member portal. Use the "log in" button at the top right of this homepage screen. Thank you. Contact Us