Data presented at the DGSM Conference in Berlin by Dr<\/em>. Christian Plettenberg on December 8, 2023<\/em> Mont-Saint-Guibert, Belgium December 11, 2023, 7:30am CET \/ 1:30am ET Nyxoah SA (Euronext Brussels\/Nasdaq: NYXH)<\/strong> (Nyxoah or the Company), a medical technology company focused on the development and commercialization of innovative solutions to treat Obstructive Sleep Apnea (OSA), today announced data from a real-world case series evaluating treatment of three complete concentric collapse (CCC) patients with the Genio\u00ae hypoglossal nerve stimulation system. The investigator-sponsored case series was presented by Dr.\u00a0Christian Plettenberg from the Universit\u00e4tsklinikum D\u00fcsseldorf on December 8, 2023. Results showed an average apnea-hypopnea index (AHI) decrease of 73% and Epworth Sleepiness Scale (ESS) decrease of 58%. There were no implant related adverse events. <\/p>\n Key Results:<\/strong><\/p>\n These data further validate Genios bilateral stimulation approach in treating CCC patients, who represent approximately 30% of HGNS eligible-to-treat OSA patients and are contraindicated to commercially available HGNS therapy in the US. European HGNS market growth accelerated with our CE-Mark CCC label expansion, and, pending FDA approval, I am excited to bring Genio to CCC patients in the US, commented Olivier Taelman, Nyxoahs Chief Executive Officer. I want to thank Dr. Plettenberg and his colleagues for their important work which reinforces Genio as a treatment solution for both non-CCC and CCC patients.<\/p>\n About Nyxoah<\/strong> Following the successful completion of the BLAST OSA study, the Genio\u00ae system received its European CE Mark in 2019. Nyxoah completed two successful IPOs: on Euronext Brussels in September 2020 and NASDAQ in July 2021. Following the positive outcomes of the BETTER SLEEP study, Nyxoah received CE mark approval for the expansion of its therapeutic indications to Complete Concentric Collapse (CCC) patients, currently contraindicated in competitors therapy. Additionally, the Company is currently conducting the DREAM IDE pivotal study for FDA and U.S. commercialization approval.<\/p>\n For more information, please visit http:\/\/www.nyxoah.com\/<\/a>.<\/p>\n Caution <\/strong> CE marked since 2019. Investigational device in the United States. Limited by U.S. federal law to investigational use in the United States.<\/p>\n Contact:<\/strong> \n Attachment<\/strong>\n<\/p>\n
Results showed an average AHI decrease of 73%<\/em><\/p>\n\n
Nyxoah is a medical technology company focused on the development and commercialization of innovative solutions to treat Obstructive Sleep Apnea (OSA). Nyxoahs lead solution is the Genio\u00ae system, a patient-centered, leadless and battery-free hypoglossal neurostimulation therapy for OSA, the worlds most common sleep disordered breathing condition that is associated with increased mortality risk and cardiovascular comorbidities. Nyxoah is driven by the vision that OSA patients should enjoy restful nights and feel enabled to live their life to its fullest.\u00a0<\/p>\n
Nyxoah<\/strong>
David DeMartino, Chief Strategy Officer
david.demartino@nyxoah.com <\/a>
+1 310 310 1313<\/p>\n\n
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