FDA Clears Lilly's Zepbound For Some Sleep Apnea Cases
The Wall Street Journal|December 23, 2024
Company said the prescription drug is only one for treating condition in adults
STEPHEN NAKROSIS
FDA Clears Lilly's Zepbound For Some Sleep Apnea Cases

Eli Lilly said the Food and Drug Administration approved Zepbound for moderate-to-severe obstructive sleep apnea in adults with obesity.

The company said Zepbound, or tirzepatide, is the first and only prescription medicine for adults suffering from this condition. The drug was launched in the U.S. for the treatment of adults with obesity or who are overweight with weight-related comorbidities in November 2023.

Bu hikaye The Wall Street Journal dergisinin December 23, 2024 sayısından alınmıştır.

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Bu hikaye The Wall Street Journal dergisinin December 23, 2024 sayısından alınmıştır.

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