Applies to Employer plans.
Covered with requirementsQualification pathways
You can qualify through any one of these.
OSA indication — moderate to severe OSA in adults with obesity
All of:
- Age ≥ 18 years
- BMI ≥ 30 kg/m2
- Sleep study within the past 12 months showing AHI ≥ 15 events per hour
- NOT diagnosed with central sleep apnea with ≥ 50% central apneas/hypopneas
- NOT diagnosed with Cheyne Stokes respiration
- Medication used as adjunct to reduced-calorie diet and increased physical activity
- Dose limited to 15 mg once weekly
- Quantity limited to 4 prefilled pens or single-dose vials per 28 days, OR 1 Kwikpen or multi-dose vial per 28 days
- Not used concurrently with other weight loss medications
Documentation to bring
- Office visit notes containing baseline body weight and BMI (≥ 30 kg/m2)
- Sleep study results within the past 12 months documenting AHI ≥ 15 events per hour
- Documentation confirming absence of central sleep apnea (≥ 50% central apneas/hypopneas) and absence of Cheyne Stokes respiration
- Medication dosage documentation
Quantity limits
- 2.5 mg, 5 mg, 7.5 mg, 10 mg, 12.5 mg, 15 mg — 4 prefilled pens or single-dose vials per 28 days, OR 1 Kwikpen or multi-dose vial per 28 days
Approval and renewal
- Initial approval: 12 months
- Renewal: every 12 months
- Renewal: ≥10% baseline body weight loss after 12 months of treatment AND stability in OSA signs or symptoms such as snoring, excessive daytime sleepiness, and fatigue AND continued adherence to reduced-calorie diet and increased physical activity AND baseline BMI ≥ 30 kg/m2 AND age ≥ 18 years.
- Renewal: At least 52 weeks on therapy before the first renewal.
Not covered when
- Central sleep apnea with ≥ 50% of central apneas/hypopneas
- Cheyne Stokes respiration
- Concurrent use with other weight loss medications (phentermine, phentermine/topiramate ER, benzphetamine, diethylpropion, phendimetrazine, Alli, Contrave, liraglutide 18 mg/3 mL pen, Qsymia, Saxenda, Xenical, Wegovy)
- All uses other than FDA-approved dosage and administration are considered investigational
- Coverage subject to benefit plan; many plans exclude weight management drugs
- This medical policy does not apply to Medicare Advantage
Policy note: OSA indication requires moderate-to-severe OSA (AHI ≥ 15 events/hour) confirmed by sleep study within 12 months. No PAP/CPAP trial required. Obesity (BMI ≥ 30) required — lower BMI threshold with comorbidity does not apply to this indication. Continuation requires ≥10% weight loss after 12 months AND OSA symptom stability. Initial authorization is 12 months (same as non-formulary exception reviews).
Policy effective April 1, 2026 · verified June 3, 2026 · source: 5.01.621 · View policy document (PDF)