Cigna: Briumvi Payer Policy (Beta Access)
HCPCS Code(s): | J2329 |
Precertification Required? | ✅ Yes (Click Here for Full Policy) |
Step Therapy Required? | Not Specified (Click Here for Full Policy) |
Provider Fax Form: | Briumvi Fax Form(✅ Available in SamaCare) |
FDA Approved Indications: |
|
Recommended Dosage: | Not Specified |
Documentation is required where noted in the criteria. Documentation may include, but not limited to, chart notes, laboratory tests, claims records, and/or other information.
Conditions Not Covered
Any other use is considered experimental, investigational, or unproven, including the following (this list may not be all-inclusive; criteria will be updated as new published data are available):
1. Concurrent Use with Other Disease-Modifying Agents Used for Multiple Sclerosis.
- These agents are not indicated for use in combination (See Appendix for examples). Additional data are required to determine if the use of disease-modifying multiple sclerosis agents in combination is safe and provides added efficacy.
Initial Approval
The patient meets all the following (i, ii, and iii):
- Patient is ≥ 18 years of age;
- AND
- Documentation the patient has a relapsing form of multiple sclerosis;
- AND
- Note: Examples of relapsing forms of multiple sclerosis include clinically isolated syndrome, relapsing remitting disease, and active secondary progressive disease. iii. Medication is prescribed by or in consultation with a neurologist or a physician who specializes in the treatment of multiple sclerosis.
Continutaion Criteria
- Patient is ≥ 18 years of age;
- AND
- Documentation the patient has a relapsing form of multiple sclerosis; AND
- Note: Examples of relapsing forms of multiple sclerosis include clinically isolated syndrome, relapsing remitting disease, and active secondary progressive disease.
- Patient meets one of the following [(1) or (2)]:
- Patient experienced a beneficial clinical response when assessed by at least one objective measure; OR
- Note: Examples include stabilization or reduced worsening in disease activity as evaluated by magnetic resonance imaging (MRI) [absence or a decrease in gadolinium enhancing lesions, decrease in the number of new or enlarging T2 lesions]; stabilization or reduced worsening on the Expanded Disability Status Scale (EDSS) score; achievement in criteria for No Evidence of Disease Activity-3 (NEDA3) or NEDA-4; improvement on the fatigue symptom and impact questionnairerelapsing multiple sclerosis (FSIQ-RMS) scale; reduction or absence of relapses; improvement or maintenance on the six-minute walk test or 12-Item Multiple Sclerosis Walking Scale; improvement on the Multiple Sclerosis Functional Composite (MSFC) score; and/or attenuation of brain volume loss.
- Patient experienced stabilization, slowed progression, or improvement in at least one symptom such as motor function, fatigue, vision, bowel/bladder function, spasticity, walking/gait, or pain/numbness/tingling sensation; AND
- Medication is prescribed by or in consultation with a neurologist or a physician who specializes in the treatment of multiple sclerosis.
Sources: https://static.cigna.com/assets/chcp/pdf/coveragePolicies/pharmacy/ip_0545_coveragepositioncriteria_ublituximab.pdf
⚠️ 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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