Eli Lilly's Zepbound Awaits FDA Approval for Sleep Apnea Treatment

TL;DR Summary
Eli Lilly has applied for FDA approval of its weight loss drug Zepbound for treating obstructive sleep apnea (OSA) and expects a decision by the end of the year. If approved, the drug could launch in early 2025. Recent trials show Zepbound significantly reduces OSA severity, potentially offering an alternative to current treatments like PAP machines.
- Eli Lilly expects FDA decision on weight loss drug Zepbound for sleep apnea as early as end of the year CNBC
- Weight-Loss Drug Zepbound Offers a New Way to Treat Sleep Apnea The New York Times
- Study identifies first drug therapy for sleep apnea Medical Xpress
- Eli Lilly seeks FDA’s OK to expand Zepbound’s uses to include sleep apnea MarketWatch
- Weight-Loss Drug Zepbound Resolves Sleep Apnea in up to 52% of Patients, Lilly Says U.S. News & World Report
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