LivaNova to Present Scientific Data at International Surgical Sleep Society 2025 Annual Meeting
Company studies continue to show durability and retention of benefits for patients receiving proximal hypoglossal nerve stimulation for moderate to severe obstructive sleep apnea
“Nearly 2 million patients with moderate to severe OSA have failed first-line therapies. These patients have a high need for an effective solution, and that is the problem
The oral and scientific poster presentations feature the research of independent investigators:
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Phenotypical Trajectories of Subjects Receiving Proximal Hypoglossal Nerve Stimulation for Obstructive Sleep Apnea: A 5-Year Analysis of the THN-3 Randomized, Controlled Trial – Oral presentation by
Alan Schwartz , M.D., Adjunct Professor of Otorhinolaryngology,Perelman School of Medicine at theUniversity of Pennsylvania , from11:00-11:08 a.m. EDT .
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Proximal Hypoglossal Nerve Stimulation Improves Sleep-Disordered Breathing, Oxygenation, and Quality of Life at One Year in Moderate to Severe Obstructive Sleep Apnea in the OSPREY Trial – Presented by
Ofer Jacobowitz , M.D., Ph.D., Otolaryngologist atENT and Allergy Associates and Clinical Professor of Otolaryngology,Zucker School of Medicine atHofstra University/Northwell Health , from1:48-1:56 p.m. EDT .
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Hypoglossal Nerve Stimulation Response Rates: Caveat Medicus (poster 31) – Presented by
Dr. Schwartz .
The symposium is titled, “The Next Generation for OSA: Proximal HGNS,” and will feature talks by
Attendees will have the opportunity to learn more about p-HGNS, a differentiated neurostimulation modality utilizing six electrodes placed on the proximal trunk of the hypoglossal nerve, offering broad access to the muscles controlling the airway through customized titration.
As announced in May of this year, the treatment arm responder rate in the OSPREY study, featuring p-HGNS, was 65% at 12 months of therapy. Responders are defined as those who realized at least a 50% improvement from the baseline apnea-hypopnea index (AHI) and an AHI value below 20.
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About THN-3 and OSPREY
Following the conclusion of LivaNova’s THN-3 clinical study (THN-3: A Randomized, Controlled Trial of Targeted Hypoglossal Nerve Stimulation for Obstructive Sleep Apnea) evaluating the aura6000™ System as a potential therapeutic option for individuals with moderate to severe OSA, the Company launched a second RCT, entitled OSPREY. Both studies evaluated a differentiated neurostimulation modality called proximal hypoglossal nerve stimulation (p-HGNS), which utilizes six electrodes placed on the proximal trunk of the hypoglossal nerve, offering broad access to the muscles controlling the airway and providing customized titration. OSPREY is a prospective, multi-center, randomized controlled open-label trial evaluating the safety and efficacy of the aura6000™ System versus a no stimulation control in subjects with moderate to severe OSA who have failed or are unwilling to use positive airway pressure treatment. CAUTION—the aura6000 System is an investigational device. Limited by Federal (or
About
Safe Harbor Statement
This news release contains “forward-looking statements” concerning the Company’s goals, beliefs, expectations, strategies, objectives, plans, underlying assumptions, and other statements that are not necessarily based on historical facts. These statements include, but are not limited to, statements regarding the THN-3 study, the OSPREY study, the aura6000™ System, p-HGNS, and presentations at upcoming conferences. Actual events may differ materially from those indicated in our forward-looking statements as a result of various factors, including those factors set forth in Item 1A of the Company’s most recent Annual Report on Form 10-K, as supplemented by any risk factors contained in Quarterly Reports on Form 10-Q and Current Reports on Form 8-K.
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