Employer / Commercial Insurance
Covered (preferred drug)What you need to qualify
- A1C of 6.5% or higher
- Lab results confirming eligibility
Qualification pathways
You can qualify through any one of these.
Initial approval - preferred agent
All of:
- Diagnosis of type 2 diabetes
- A1C >= 6.5% confirmed by lab test (lab results or medical records required)
- Requested agent is a preferred agent
- Patient age within FDA labeling for the requested indication, or support for off-label age use
- Patient will NOT use requested agent in combination with a DPP-4 containing agent
- Patient will NOT use requested agent in combination with another GLP-1 receptor agonist
- Patient does NOT have any FDA labeled contraindications to the requested agent
Continuation of therapy
All of:
- Diagnosis of type 2 diabetes
- A1C >= 6.5% confirmed by lab test (lab results or medical records required)
- Patient will NOT use requested agent in combination with a DPP-4 containing agent
- Patient will NOT use requested agent in combination with another GLP-1 receptor agonist
- Patient does NOT have any FDA labeled contraindications to the requested agent
Plus any one of:
- Patient has been treated with a preferred agent within the past 90 days (not starting on samples)
- Prescriber states patient has been treated with a preferred agent within the past 90 days (not starting on samples) AND patient is at risk if therapy with a preferred agent is discontinued
Documentation to bring
- Documentation of type 2 diabetes diagnosis
- Lab results confirming A1C >= 6.5% (or medical records)
- For continuation: documentation of prior preferred agent use within past 90 days, or prescriber attestation with clinical risk justification
- Documentation that patient will not use requested agent with a DPP-4 inhibitor
- Documentation that patient will not use requested agent with another GLP-1 receptor agonist
Quantity limits
- 2.5 MG/0.5ML
- 5 MG/0.5ML, 7.5 MG/0.5ML, 10 MG/0.5ML, 12.5 MG/0.5ML, 15 MG/0.5ML — 4 pens
Approval and renewal
- Initial approval: 12 months
- Renewal: every 12 months
Not covered when
- Combination use with DPP-4 containing agents (e.g., Januvia, Janumet, Tradjenta, Onglyza, Nesina, Alogliptin/metformin, Alogliptin/pioglitazone, Brynovin, Janumet XR, Jentadueto, Jentadueto XR, Kombiglyze XR, Trijardy, Zituvio, Zituvimet, Zituvimet XR)
- Combination use with another GLP-1 receptor agonist (e.g., Saxenda, Wegovy, Zepbound, Bydureon, Byetta, Exenatide, Ozempic, Rybelsus, Trulicity, Victoza)
- FDA labeled contraindications to the requested agent (including personal/family history of MTC or MEN 2, prior serious hypersensitivity to active ingredient or components)
Policy note: Mounjaro is listed as a preferred agent on this formulary. Non-preferred agents (e.g., Victoza) require trials of TWO preferred agents (semaglutide/Ozempic or Rybelsus, dulaglutide/Trulicity, tirzepatide/Mounjaro) with inadequate response, intolerance, hypersensitivity, or FDA labeled contraindication. Step therapy exemption may apply if a prior health plan paid for the medication — documentation of a paid claim may be required. The 2.5 mg dose has a special QL: 4 pens per 180 days; for maintenance use exceeding the QL, patient must demonstrate inability to use an FDA labeled maintenance strength AND clinical benefit from the lower strength.
Policy effective February 1, 2026 · verified June 2, 2026 · source: ALBP_GLP-1_Agonists_PAQL_ProgSum.pdf