Actimmune (interferon gamma-1b)

Indications for Prior Authorization

Actimmune (interferon gamma-1b)
  • For diagnosis of Chronic Granulomatous Disease (CGD)
    Indicated for reducing the frequency and severity of serious infections associated with Chronic Granulomatous Disease (CGD).

  • For diagnosis of Severe Malignant Osteopetrosis (SMO)
    Indicated for delaying time to disease progression in patients with severe, malignant osteopetrosis (SMO).

Criteria

Actimmune

Prior Authorization (Initial Authorization)

Length of Approval: 12 Month(s)

  • Diagnosis of one of the following:
    • Chronic granulomatous disease (CGD)
    • Severe, malignant osteopetrosis (SMO)
Actimmune

Prior Authorization (Reauthorization)

Length of Approval: 12 Month(s)

  • Patient does not show evidence of progressive disease while on therapy
P & T Revisions

2025-04-02, 2024-04-03, 2023-04-11, 2022-04-04, 2021-09-27, 2021-05-25, 2021-04-02, 2020-03-03

  1. Actimmune Prescribing Information. Horizon Therapeutics USA, Inc. Deerfield, IL. March 2021.

  • 2025-04-02: 2025 Annual Review. No criteria changes.
  • 2024-04-03: 2024 Annual Review. No criteria changes.
  • 2023-04-11: Annual review
  • 2022-04-04: Annual review - reformatted criteria without changing clinical intent. Updated background and references.
  • 2021-09-27: Addition of EHB formulary to guideline, no changes to criteria
  • 2021-05-25: Addition of EHB formulary to guideline, no changes to criteria
  • 2021-04-02: Annual Review
  • 2020-03-03: Annual reviews

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