Applies to Employer plans.
Covered with requirementsQualification pathways
You can qualify through any one of these.
CV risk reduction in adults with established CVD and obesity/overweight
All of:
- Requested use is to reduce the risk of major adverse cardiovascular events (cardiovascular death, non-fatal MI, or non-fatal stroke) in adults with established cardiovascular disease and either obesity or overweight
- Requested agent is Wegovy
- Patient has a pretreatment BMI ≥ 27 kg/m2
- Patient will use optimized pharmacotherapy for established cardiovascular disease in combination with Wegovy
- Patient does NOT have any FDA labeled contraindications
Plus any one of:
- History of myocardial infarction
- History of stroke
- Peripheral artery disease as defined by intermittent claudication with ankle-brachial index < 0.85 at rest, or peripheral arterial revascularization procedure, or amputation due to atherosclerotic disease
Documentation to bring
- Documentation of established cardiovascular disease (CAD, ACS, history of MI, angina, revascularization, PCI/CABG, stroke, TIA, carotid or arterial stenosis, PAD including aortic aneurysm, all of atherosclerotic origin)
- Documentation of qualifying CV event: MI, stroke, or PAD (with ABI < 0.85, revascularization, or amputation due to atherosclerotic disease)
- Baseline BMI documentation (≥ 27 kg/m2)
- Documentation of current or planned optimized pharmacotherapy for established cardiovascular disease
Quantity limits
- 0.25 MG/0.5ML, 0.5 MG/0.5ML, 1 MG/0.5ML — 8 pens per 180-day supply (84-day)
- 1.7 MG/0.75ML, 2.4 MG/0.75ML — 4 pens per 28-day supply
- 7.2 MG/0.75ML — 4 pens per 28-day supply
- 1.5 MG tablet, 4 MG tablet, 9 MG tablet — 60 tablets per 180-day supply (84-day)
- 25 MG tablet — 30 tablets per 30-day supply
Approval and renewal
- Initial approval: 12 months
- Renewal: every 12 months
- Renewal: At renewal, patient must have had clinical benefit with Wegovy AND will continue optimized pharmacotherapy for established cardiovascular disease. Initial qualifying CV event documentation and BMI threshold are not explicitly re-verified at renewal.
Not covered when
- Any FDA labeled contraindications to the requested agent
Exceptions
- BCBS_NM_Fully_Insured_or_HIM: May be approved if patient does not have FDA labeled contraindications AND the requested indication is a rare disease AND patient has another FDA labeled indication or compendia-supported indication.
- Ohio_Fully_Insured_or_HIM_SHOP: May be approved if member resides in Ohio, plan is Fully Insured or HIM Shop (SG), no FDA labeled contraindications, AND patient has another FDA labeled or compendia-supported indication OR prescriber submits two articles from major peer-reviewed journals.
Policy note: Established CVD is defined broadly as: CAD, ACS, history of MI, stable or unstable angina, coronary or other arterial revascularization, prior PCI/CABG, stroke, TIA, carotid or other arterial stenosis, or PAD including aortic aneurysm, all of atherosclerotic origin. The PAD qualifying criterion specifically requires: intermittent claudication with ABI < 0.85 at rest, OR peripheral arterial revascularization procedure, OR amputation due to atherosclerotic disease. GDMT specified as 'optimized pharmacotherapy for established cardiovascular disease' without naming specific drug classes.
Policy effective May 18, 2026 · verified June 2, 2026 · source: Hcsc Weight Management Prog Sum · View policy document (PDF)