Nyxoah תשתתף בכנס הבריאות השנתי ה-36 של פייפר סנדלר
מונט-סנט-גיברט, בלגיה, 20 בנובמבר 2024, (GLOBE NEWSWIRE) :
Nyxoah SA (נאסד"ק/יורונקסט בריסל: NYXH) ("Nyxoah" או "החברה"), חברת טכנולוגיות רפואיות המפתחת חלופות טיפול פורצות דרך לדום נשימה בשינה (OSA) באמצעות נוירומודולציה, הודיעה היום כי החברה תשתתף בכנס הבריאות השנתי ה-36 של פייפר סנדלר ביום רביעי, 4 בדצמבר 2024. החברה אמורה להציג בשעה 14:00 ET באותו יום באמצעות שידור אינטרנט.
Nyxoah to Participate in the Piper Sandler 36th Annual Healthcare Conference
Mont-Saint-Guibert (Belgium), November 20, 2024, (GLOBE NEWSWIRE):
Nyxoah SA (Euronext Brussels/Nasdaq: NYXH) (“Nyxoah” or the “Company”), a medical technology company that develops breakthrough treatment alternatives for Obstructive Sleep Apnea (OSA) through neuromodulation, today announced that the Company will participate in the Piper Sandler 36th Annual Healthcare Conference on Wednesday, December 4, 2024. The Company is scheduled to present at 2:00pm ET the same day via webcast.
A live audio webcast of the presentation will be available online at the investor relations page of the Company’s website at investors.nyxoah.com.
About Nyxoah
Nyxoah is reinventing sleep for the billion people that suffer from obstructive sleep apnea (OSA). We are a medical technology company that develops breakthrough treatment alternatives for OSA through neuromodulation. Our first innovation is Genio®, a battery-free hypoglossal neuromodulation device that is inserted through a single incision under the chin and controlled by a wearable. Through our commitment to innovation and clinical evidence, we have shown best-in-class outcomes for reducing OSA burden.
Following the successful completion of the BLAST OSA study, the Genio® 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 announced positive outcomes from the DREAM IDE pivotal study for FDA and U.S. commercialization approval.
Caution – CE marked since 2019. Investigational device in the United States. Limited by U.S. federal law to investigational use in the United States.
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Contacts:
Nyxoah John Landry, CFO [email protected]
For Media In United States FINN Partners – Glenn Silver [email protected]
In Belgium/France Backstage Communication – Gunther De Backer [email protected]
In International/Germany MC Services – Anne Hennecke [email protected]
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