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: |
|
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:
- The member has a diagnosis of neovascular (wet) age-related macular degeneration.
- The member has previously responded (within the last 6 months) to at least two intravitreal injections of a VEGF inhibitor (e.g., Avastin, Eylea).
- Susvimo must be used with the Susvimo ocular implant.
Continuation Criteria
Authorization for 12 months may be granted if:
- The member is currently receiving therapy with Susvimo.
- 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: |
|
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. |
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:
- The member has a diagnosis of neovascular (wet) age-related macular degeneration (AMD).
- The member has failed, has a contraindication to, or is intolerant of bevacizumab (Avastin).
- Susvimo is being used with the Susvimo ocular implant.
Continuation Criteria:
Authorization is considered medically necessary for 12 months if:
- The member is currently receiving therapy with Susvimo.
- 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.
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