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Biologic Immunomodulators - Tremfya Prior Authorization Criteria - Medicare Part D

Medicare Utilization Management Policy
Version Date: 02/01/2025

Prior Authorization Criteria for Approval

Initial Evaluation

Tremfya will be approved when ALL of the following are met:

  1. The patient has an FDA labeled indication for the requested medication
    AND
  2. ONE of the following:
    1. There is evidence of a claim that the patient is currently being treated with the requested medication within the past 90 days
      OR
    2. The prescriber states the patient is currently being treated with the requested medication AND provided clinical justification to support that the patient is at risk if therapy is changed
      OR
    3. The patient’s medication history indicates use of another biologic immunomodulator medication for the same FDA labeled indication
      OR
    4. The patient’s diagnosis does NOT require a conventional prerequisite agent*
      OR
    5. The patient’s medication history indicates use of ONE formulary conventional prerequisite medication for the requested indication*
      OR
    6. The patient has an intolerance or hypersensitivity to at least ONE formulary conventional prerequisite medication for the requested indication*
      OR
    7. The patient has an FDA labeled contraindication to at least ONE formulary conventional prerequisite medication for the requested indication* 
      AND
  3. The patient does NOT have any FDA labeled contraindications to the requested medication
    AND
  4. The patient will NOT be using the requested medication in combination with another biologic immunomodulator
    AND
  5. The requested dose is within FDA labeled dosing for the requested indication

*NOTE:

  • Use of ONE conventional prerequisite agent is required for diagnoses of plaque psoriasis or moderate ulcerative colitis
  • NO prerequisites are required for diagnoses of psoriatic arthritis or severe ulcerative colitis
  • Formulary conventional medications for plaque psoriasis include acitretin, calcipotriene, cyclosporine, methotrexate, tacrolimus, tazarotene, or topical corticosteroids
  • Formulary conventional medications for moderate ulcerative colitis include: balsalazide, mesalamine, sulfasalazine, mercaptopurine, azathioprine, and corticosteroids (including budesonide EC capsule)

Length of approval: 12 months

Renewal Evaluation

Tremfya will be approved for renewal when ALL of the following are met:

  1. The patient has been previously approved for the requested medication through the plan’s Prior Authorization criteria
    AND
  2. The patient has an FDA labeled indication for the requested medication AND
  3. The patient has had clinical improvement (slowing of disease progression or decrease in symptom severity and/or frequency)
    AND
  4. The patient does NOT have any FDA labeled contraindications to the requested medication
    AND
  5. The patient will NOT be using the requested medication in combination with another biologic immunomodulator
    AND
  6. The requested dose is within FDA labeled dosing for the requested indication

Length of approval: 12 months