FDA approves Lilly drug for obstructive sleep apnea

23 December 2024

US pharma major Eli Lilly (NYSE: LLY) today announced the US Food and Drug Administration (FDA) approved Zepbound its (tirzepatide) as the first and only prescription medicine for adults with moderate-to-severe obstructive sleep apnea (OSA) and obesity.

Lilly’s shares edged up 1.6% to $780.31 on the news.

OSA occurs when a person’s upper airway becomes blocked, causing pauses in breathing during sleep. While OSA can affect anyone, it is more common in people who have overweight or obesity.

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