Aetna: Susvimo Payer Policy

Created by C. Denise Burrell, Modified on Wed, 8 Jan at 1:48 PM by C. Denise Burrell

Aetna: Susvimo Payer Policy (Beta Access)

TABLE OF CONTENTS


 MEDICARE PART B


HCPCS Code(s):J2779
Precertification Required?Yes (Click Here for Full Policy)
Step Therapy Required? Yes (Click Here for Full Policy)
Provider Fax Form:Susvimo Fax Form (✅ Available in SamaCare)
FDA Approved Indications:
  • Neovascular (wet) Age-related Macular Degeneration (AMD)
    • For patients who have previously responded to at least two intravitreal injections of a Vascular Endothelial Growth Factor (VEGF) inhibitor medication.
Recommended Dosage:

Not Specified


Note: Susvimo must be used in conjunction with the Susvimo ocular implant.


Initial Approval Criteria

Authorization of 12 months may be granted for treatment of neovascular (wet) age-related macular degeneration when the following criteria are met:

  1. The member has a diagnosis of neovascular (wet) age-related macular degeneration.
  2. The member has previously responded (within the last 6 months) to at least two intravitreal injections of a VEGF inhibitor (e.g., Avastin, Eylea).
  3. Susvimo must be used with the Susvimo ocular implant.


Continuation Criteria

Authorization for 12 months may be granted if:

  1. The member is currently receiving therapy with Susvimo.
  2. Susvimo is being used to treat an approved indication.The medication has been effective for treating the diagnosis or condition.

Sources: 

https://www.aetna.com/content/dam/aetna/pdfs/aetnacom/healthcare-professionals/documents-forms/Susvimo-5046-A-Aetna-MedB.pdf

https://www.aetna.com/content/dam/aetna/pdfs/aetnacom/healthcare-professionals/documents-forms/VEGF-Inhibitors-for-ocular-indications-1031-AMBST.pdf



COMMERCIAL

HCPCS Code(s):J2779
Precertification Required?✅ Yes (Click Here For Full Policy)
Step Therapy Required?  Yes (Click Here For Full Policy)
Provider Fax Form: Susvimo Fax Form (✅ Available in SamaCare)
FDA Approved Indications:
  • Neovascular (wet) age-related macular degeneration (AMD) 
Recommended Dosage:

Ranibizumab injection is available as Susvimo 100 mg/mL solution in a single-dose vial for intravitreal use via ranibizumab (Susvimo) ocular implant.

Neovascular (wet) age-related macular degeneration (AMD):

The recommended dose is ranibizumab injection (Susvimo) 2 mg (0.02 mL of 100 mg/mL solution) continuously delivered via the Susvimo implant with refills every 24 weeks (approximately 6 months).

Supplemental treatment with 0.5 mg intravitreal ranibizumab injection may be administered in the affected eye if clinically necessary.

Initial implantation, refill-exchange, and implant removal (if necessary) require strict aseptic conditions.

Note: Susvimo is considered medically necessary only after failure, contraindication, or intolerance to bevacizumab (Avastin). 

Other Pertinent Information

  • Susvimo must be used with the Susvimo ocular implant.
  • Susvimo is considered more costly than Avastin and is only approved when there is a contraindication, intolerance, or failure of Avastin.


  • Exclusion(s):
    • All other indications not listed above are considered not medically necessary

Initial Approval Criteria

Authorization is considered medically necessary for 12 months when the following criteria are met:

  1. The member has a diagnosis of neovascular (wet) age-related macular degeneration (AMD).
  2. The member has failed, has a contraindication to, or is intolerant of bevacizumab (Avastin).
  3. Susvimo is being used with the Susvimo ocular implant.


Continuation Criteria:

Authorization is considered medically necessary for 12 months if:

  1. The member is currently receiving therapy with Susvimo.
  2. There is documentation of positive clinical responseto therapy, such as:
    • Improvement or maintenance of best corrected visual acuity (BCVA).


Sources:

⚠️ Disclaimer: This article is a policy summary and does not guarantee coverage or approval. 

Policies may vary based on plan, payer-specific rules, state or regional requirements, benefit structure, formulary placement, and patient-specific considerations like diagnosis or clinical history. Always review the full policy and confirm details directly with the payer to ensure compliance. 


 

We're here to guide you through your prior authorization quest!





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