Employer / Commercial Insurance
Covered (preferred drug)What you need to qualify
- A1C of 6.5% or higher
- Diagnosis documented with a code (E11.10, E11.11, E11.9, E11.65, E11.69, E11.00, E11.01, E11.641, E11.21, E11.22, E11.29, E11.311, E11.319, E11.39, E11.36, E11.40, E11.49, E11.610, E11.51, E11.59, E11.618, E11.620, E11.628, E11.630, E11.638, E11.649, E11.8, E13.37X1, E13.37X2, E13.37X3, E13.37X4, E13.37X5, E13.37X6, E13.37X7, E13.37X8, E13.37X9, E13.10)
- Lab results confirming eligibility
Qualification pathways
You can qualify through any one of these.
Initial approval for T2DM
All of:
- Individual is being treated as an adjunct to diet and exercise for a diagnosis of type 2 diabetes
- Diagnosis confirmed by lab tests (e.g., A1C >= 6.5%)
- Individual is new to therapy
- Individual will NOT use the requested agent in combination with a DPP-4 containing agent
- Individual will NOT use the requested agent in combination with another GLP-1 receptor agonist
- Individual does NOT have any FDA labeled contraindications to the requested agent
Continuation of therapy
All of:
- Individual is being treated as an adjunct to diet and exercise for a diagnosis of type 2 diabetes
- Diagnosis confirmed by lab tests (e.g., A1C >= 6.5%)
- Requested medication is eligible for continuation of therapy
- Individual will NOT use the requested agent in combination with a DPP-4 containing agent
- Individual will NOT use the requested agent in combination with another GLP-1 receptor agonist
- Individual does NOT have any FDA labeled contraindications to the requested agent
Plus any one of:
- Documentation that the individual has been treated with the requested medication within the past 90 days
- Prescriber states the individual has been treated with the requested medication within the past 90 days and is at risk if therapy is discontinued
Documentation to bring
- Lab test results confirming T2DM diagnosis (e.g., A1C >= 6.5%) or medical records
- For continuation: documentation of treatment with requested medication within the past 90 days, OR prescriber attestation of same with clinical risk statement
Approval and renewal
- To renew, the plan looks for For continuation, ONE of the following: documentation that the individual has been treated with the requested medication within the past 90 days, OR prescriber states the individual has been treated with the requested medication within the past 90 days and is at risk if therapy is discontinued.
Not covered when
- Combination use with DPP-4 containing agents (e.g., Glyxambi, Januvia, Janumet, Jentadueto, Kazano, Kombiglyze, Nesina, Onglyza, Tradjenta)
- Combination use with another GLP-1 receptor agonist
- FDA labeled contraindications to the requested agent
- Use of samples will not be considered current or stable therapy
Exceptions
- State Health Plan (State and School Employees): Prescription drug may be covered under a prescription drug benefit plan administered by the State Health Plan's Pharmacy Benefit Manager. PA requests must be submitted to the Plan's PBM (CVS Caremark) at https://www.dfa.ms.gov/cvs-caremark
- Structural Steel Self-Insured Group (FID#: 89805, Formulary: BCBSMS COMM-CUSTOM STEEL): Effective 06/16/2025, all GLP-1 agonist medications are covered without Prior Authorization.
Policy note: Effective 04/01/2026, review at the pharmacy is required for new start GLP-1 agonist prescriptions. Prior authorization is required for members with type 2 diabetes not treated with an oral antidiabetic agent. The metformin trial requirement was removed effective 04/01/2026. The policy covers Ozempic under the same criteria as Mounjaro, Rybelsus, and Trulicity. Although Ozempic has FDA labeling for CV risk reduction and CKD indications, this policy only establishes PA criteria under the T2DM indication context; those expanded indications are not separately addressed in the criteria section. BCBSMS determines medication trial and adherence by pharmacy claims data over the preceding 12 months.
Policy effective April 1, 2026 · verified July 26, 2026 · source: policy-231.html