71% median AHI reduction in OSA patients after 12 months with Nyxoah's Genio® device in the DREAM U.S. pivotal study.

Nyxoah's DREAM U.S. pivotal study revealed a 71% median reduction in the Apnea-Hypopnea Index (AHI) for patients with obstructive sleep apnea (OSA) after 12 months. Notably, 82% of participants had an AHI below 15, enhancing their quality of life. Nyxoah's Genio® device, a battery-free hypoglossal neuromodulation system, is now advancing toward FDA approval, promising a new treatment option for OSA patients in the U.S.

September 27, 2024
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