Medicaid
Covered with requirementsWhat you need to qualify
- BMI of 27 or higher
- Prior trial of another GLP-1 medication (Ozempic)
- Prescribed by or in consultation with a specialist
- Established cardiovascular disease (MI, stroke, and PAD)
- On guideline-directed medical therapy (optimized pharmacotherapy for established cardiovascular disease per current consensus guidelines)
Qualification pathways
You can qualify through any one of these.
Initial approval — Wegovy for CV risk reduction (non-preferred)
All of:
- Prescribed by or in consultation with an appropriate specialist (e.g., cardiologist, vascular surgeon, neurologist)
- Recent BMI >= 27 kg/m2
- Used in combination with optimized pharmacotherapy for established CVD per current consensus guidelines unless contraindicated or not tolerated
- Used in combination with lifestyle changes and behavioral modifications
- Age-appropriate per FDA labeling, compendia, or peer-reviewed literature
- No contraindication to the prescribed drug
- History of therapeutic failure of, OR contraindication to, OR intolerance to the maximum FDA-approved dose of Ozempic (semaglutide) — OR for Wegovy 2.4 mg: dose titration to semaglutide 2 mg completed plus medical reason for 2.4 mg dose
Plus any one of:
- Prior myocardial infarction
- Prior stroke
- Peripheral arterial disease with: intermittent claudication with ankle-brachial index < 0.85 at rest, OR history of peripheral arterial revascularization, OR history of amputation due to atherosclerotic disease
Documentation to bring
- Documentation of specialist prescribing or consultation (cardiologist, vascular surgeon, or neurologist)
- Recent BMI documentation (>= 27 kg/m2)
- Documentation of qualifying CV event: prior MI, prior stroke, or PAD with claudication (ABI <0.85), revascularization history, or amputation due to atherosclerotic disease
- Documentation of current optimized pharmacotherapy for CVD per consensus guidelines, or reason it is contraindicated/not tolerated
- Documentation of therapeutic failure of Ozempic (semaglutide) at maximum FDA-approved dose, OR contraindication or intolerance to Ozempic (with chart documentation of troubleshooting attempts over at least 1 month if intolerance-based)
- For Wegovy 2.4 mg: documentation that dose titration to semaglutide 2 mg has been completed and medical reason supporting need for 2.4 mg dose — OR documentation of therapeutic failure of Ozempic at maximum dose
- Documentation of age-appropriateness per FDA labeling, compendia, or peer-reviewed literature
- Documentation of no contraindication to the prescribed drug
- If therapeutic duplication: documentation of intent to transition or medical reason for concomitant use supported by literature/guidelines
Approval and renewal
- Initial approval: 6 months
- Renewal: every 6 months
- To renew, the plan looks for Renewal requires: (1) prescribed by or in consultation with appropriate specialist (cardiologist, vascular surgeon, neurologist); (2) used in combination with optimized pharmacotherapy for established CVD per current consensus guidelines unless contraindicated or not tolerated; (3) continued lifestyle changes and behavioral modifications; (4) no contraindication; (5) step-therapy requirement maintained (therapeutic failure/contraindication/intolerance to Ozempic max dose). BMI and qualifying CV event documentation not explicitly re-verified at renewal per renewal guidelines as stated, but specialist and GDMT requirements are re-checked.
Not covered when
- Overweight/obesity treatment indication excluded
- Saxenda (liraglutide) not covered for any indication
Policy note: Wegovy is non-preferred for all non-diabetes indications. For CV risk reduction, the step-therapy requirement is therapeutic failure of/contraindication to/intolerance to the maximum FDA-approved dose of Ozempic (semaglutide). PAD qualifying criteria are specific: requires at least one of intermittent claudication with ABI <0.85 at rest, history of peripheral arterial revascularization, or amputation due to atherosclerotic disease. For Wegovy 2.4 mg strength specifically, an alternative pathway exists: prior therapeutic failure of Ozempic at max dose OR (completed titration to semaglutide 2 mg plus medical reason for 2.4 mg). All non-OSA/non-MASH non-diabetes indications require a recent 6-month trial of lifestyle changes and behavioral modifications OR medical reason why immediate treatment is necessary at initial request. For CV and MASH, lifestyle changes are required but the 6-month prior trial requirement does not apply — concurrent lifestyle modification suffices. Prescriptions limited to 1-month supply per fill. Approval duration up to 6 months for non-diabetes, non-OSA indications.
Policy effective January 1, 2026 · verified June 4, 2026 · source: mab2025112403.pdf