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ProSomnus, Inc. (NASDAQ:OSA) (the "Company"), the leading non-CPAP Obstructive Sleep Apnea (OSA) therapy™, today announced the publication of a study by the Cureus Journal of Medical Science, in which the Company's precision oral appliance therapy (OAT) devices successfully treated patients' OSA.
"The study underscored what we see daily in our practice at Star Sleep & Wellness. Our team continues to favor the ProSomnus® EVO® Sleep and Snore Device, as it not only garners the fewest number of patient complaints regarding fit and comfort, but also shows to be superior in resolving chief complaints such as partner discontent, fatigue and daytime sleepiness," said Dr. Kent Smith, D-ABDSM, ASBA, a co-author of the study.
Key findings from the study, titled "Evaluating the Clinical Performance of a Novel, Precision Oral Appliance Therapy Medical Device Made Wholly from a Medical Grade Class VI Material for the Treatment of Obstructive Sleep Apnea," include:
"Oral appliance success is traditionally evaluated with the AHI metrics. My experience with the ProSomnus® EVO® precision oral appliance is that it exceeds the American Academy of Sleep Medicine (AASM) and the American Academy of Dental Sleep Medicine (AADSM) standards for efficacy. This study shows that residual AHI using an EVO device is superior to other oral appliances, and superior to hypoglossal nerve stimulation in reducing the AHI. Clinically speaking, I have delivered over 300 EVO devices. I find EVO to have great patient compliance, minimal delivery adjustments, and overall better patient comfort than other traditional oral appliances for sleep apnea," said John A. Carollo, DMD, D-ABDSM, D-ASBA, a co-author of the study.
"My experience with ProSomnus began in 2019 and since that time, I have come to appreciate the benefit to my patients in delivering precision oral appliances such as these. The study irrefutably demonstrates this," said Dr. Aditi Desai, BDS, MSc, FCGDent, a co-author of the study. "The ethos of the company has certainly helped drive the field of oral appliance therapy as a most credible alternative to CPAP."
ProSomnus also announced additional clinical research highlighting the efficacy, decreased AHI incidents, and strong therapy adherence associated with the Company's precision OAT devices:
"In an effort to offer patients an effective titration schedule, the bite registration is generally made at the so called maximal comfortable protrusion, minus 2.0 mm after DISE investigation. In a retrospective analysis of this procedure at 6 general hospitals, the reduction in Obstructive Apnea-Hypopnea index, as measured with type 3 polygraphy, was highly significant lowered to 3.9 events/hr sleep, irrespective of the sleep center methodology used," said Prof. Dr. Marc Braem, DDS, PhD.
"These studies demonstrate that precision oral devices offer consistent efficacy across multiple clinical and hospital settings, and are associated with reliable adherence. Traditional oral devices are typically associated with inconsistent efficacy due to imprecise repositioning and stabilization of the jaw and unreliable durability due to side effects and mechanical issues," said Len Liptak, ProSomnus Chief Executive Officer. "This new data adds to a body of evidence underscoring that ProSomnus devices are a safe and efficacious option for millions of OSA patients who have terminated or refused CPAP, or been impacted by the CPAP recall."
Posted In: OSA