Syfovre (pegcetacoplan)
Indications for Prior Authorization
Syfovre (pegcetacoplan)
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For diagnosis of Geographic Atrophy (GA)
Indicated for the treatment of geographic atrophy (GA) secondary to age-related macular degeneration (AMD).
Criteria
Syfovre
Prior Authorization (Initial Authorization)
Length of Approval: 12 Month(s)
- Diagnosis of geographic atrophy (GA) secondary to age-related macular degeneration (AMD) as confirmed by one of the following:
- Fundus photography (e.g. fundus autofluorescence [FAF])
- Optical coherence tomography (OCT)
- Fluorescein angiography
- Prescribed by or in consultation with an ophthalmologist experienced in the treatment of retinal diseases
Syfovre
Prior Authorization (Reauthorization)
Length of Approval: 12 Month(s)
- Patient demonstrates positive clinical response to therapy (e.g., reduction in growth rate of GA lesion)
P & T Revisions
2024-06-18, 2024-03-13, 2023-10-16, 2023-06-16, 2023-04-14
References
- Syfovre Prescribing Information. Apellis Pharmaceuticals, Inc. Waltham, MA. November 2023.
Revision History
- 2024-06-18: Removed criterion "GA is not secondary to any other conditions."
- 2024-03-13: 2024 Annual review. No changes to clinical content. Updated references.
- 2023-10-16: Program update to standard reauthorization language. No changes to clinical intent.
- 2023-06-16: Attached EHB formulary.
- 2023-04-14: New program for Syfovre.