Zepbound for obstructive sleep apnea

FDA-approved for obstructive sleep apnea

The short answer

Zepbound (tirzepatide) became the first GLP-1-class drug FDA-approved for moderate-to-severe obstructive sleep apnea in adults with obesity (December 2024).

Zepbound specifically

FDA-approved (Dec 2024) for moderate-to-severe OSA in adults with obesity — the SURMOUNT-OSA trial showed major AHI reductions.

BMI & eligibility

The Zepbound OSA indication requires obesity. Other GLP-1s remain off-label for OSA and qualify through the obesity pathway (BMI ≥30, or ≥27 with comorbidity).

Check your BMI

BMI calculator

Overweight27.7

BMI 27-29.9 — eligible if comorbidity (T2D, hypertension, sleep apnea, PCOS).

BMI is one signal among several. Waist circumference, body composition, metabolic markers, and clinical history also matter — talk to a prescriber.

Insurance & coverage

Zepbound now has a direct OSA pathway — a sleep study confirming moderate-to-severe OSA plus obesity supports prior authorization. Other GLP-1s require an obesity-based PA.

Check if your plan covers it

We earn affiliate commissions from listed providers. See our editorial standards.

Other GLP-1s for obstructive sleep apnea

Zepbound for other conditions

See all GLP-1 eligibility guides

Sources

Educational information, not medical advice. FDA-approval status reflects labeling as of 2026; off-label prescribing is legal and common but coverage varies.