You can qualify through any one of these.
Initial Approval – OSA (without concurrent T2DM)
All of:
- Diagnosis of moderate to severe OSA confirmed by polysomnography or home sleep apnea test within past 12 months with AHI >= 15 respiratory events per hour
- Age >= 18 years
- BMI >= 30 kg/m2
- Member does not have central or mixed sleep apnea
- Active enrollment in physician-directed weight loss program for at least 6 months involving reduced calorie diet, increased physical activity, and behavioral modification, with plan to continue enrollment while on Zepbound
- Zepbound not prescribed concurrently with other tirzepatide-containing products or any other GLP-1 receptor agonist
- Documentation of member's baseline body weight in kg
- Dose does not exceed escalation schedule (2.5mg wk1-4, 5mg wk5-8, 7.5mg wk9-12, 10mg wk13-16, 12.5mg wk17-20, 15mg wk21-24) and quantity limit (1 pen/vial per week for single-dose or 1 vial/KwikPen every 4 weeks for multi-dose)
Plus any one of:
- Member has continued symptoms of OSA despite adherence to PAP therapy (>=4 hours/night for >=70% of nights)
- Member is not a candidate for PAP therapy (e.g., upper airway anatomic abnormalities)
Initial Approval – OSA with concurrent T2DM (Illinois HIM: step therapy waived as of 1/1/2026)
All of:
- Diagnosis of moderate to severe OSA confirmed by polysomnography or home sleep apnea test within past 12 months with AHI >= 15 respiratory events per hour
- Age >= 18 years
- BMI >= 30 kg/m2
- Member does not have central or mixed sleep apnea
- Concurrent diagnosis of type 2 diabetes mellitus
- Member has received optimal diabetic standard of care therapy as evidenced by a trial of >= 3 consecutive months each of ALL of: (1) Ozempic or Rybelsus, (2) Trulicity, and (3) liraglutide (generic Victoza), unless clinically significant adverse effects are experienced or all are contraindicated
- If member is currently on a GLP-1 receptor agonist and requesting switch to Zepbound, medical justification supports necessity (intolerance due to common GI adverse effects is NOT acceptable justification)
- Active enrollment in physician-directed weight loss program for at least 6 months involving reduced calorie diet, increased physical activity, and behavioral modification, with plan to continue enrollment while on Zepbound
- Zepbound not prescribed concurrently with other tirzepatide-containing products or any other GLP-1 receptor agonist
- Documentation of member's baseline body weight in kg
- Dose does not exceed escalation schedule and quantity limit
Plus any one of:
- Member has continued symptoms of OSA despite adherence to PAP therapy (>=4 hours/night for >=70% of nights)
- Member is not a candidate for PAP therapy (e.g., upper airway anatomic abnormalities)
Policy effective December 20, 2024 · verified June 2, 2026 · source: CP.PMN.298.pdf