PLEASANTON, Calif., May 30, 2023 (GLOBE NEWSWIRE) — ProSomnus, Inc. (“the Company”) (NASDAQ: OSA), a leading CPAP alternative for the treatment of Obstructive Sleep Apnea (OSA), announced the presentation of four abstracts at the 2023 American Academy of Dental Sleep Medicine (AADSM) Annual Meeting, held May 19-21 in Philadelphia, Pennsylvania, and two abstracts at the American Thoracic Society (ATS) 2023 International Conference, held May 19-24 in Washington, D.C.
The data presented at both meetings demonstrate that ProSomnus’s Precision OAT devices are:
“The growing body of clinical evidence continues to show that Precision Oral Appliance Therapy is more efficacious and even safer than legacy treatment options,” said John E. Remmers, MD, Chief Scientist of ProSomnus. “These particular studies not only demonstrate efficaciousness but additional benefits for patients, such as better adherence and fewer adverse events.”
Data from the First Line Obstructive Sleep Apnea Treatment Study (FLOSAT) study, a clinical trial comparing the clinical effectiveness of OAT and CPAP were presented at both meetings:
In addition, key findings were also presented in the following posters at AADSM:
At ATS 2023, further data were presented in the following poster:
“Precision oral appliance therapy consists of intraoral medical devices that precisely track to the healthcare provider’s treatment plan and the patient’s anatomy,” said Len Liptak, Chief Executive Officer of ProSomnus. “This data further validates that our non-invasive, patient-preferred, precision oral appliance therapy is associated with excellent outcomes for patients with OSA.”
About ProSomnus
ProSomnus (NASDAQ: OSA) is a leading CPAP alternative for the treatment of Obstructive Sleep Apnea, a serious medical disease affecting over 1 billion people worldwide, that is associated with comorbidities including heart failure, stroke, hypertension, morbid obesity, and type 2 diabetes. ProSomnus intraoral medical devices are engineered to precisely track the treatment plan and anatomy for each patient. Non-invasive, patient preferred and easy to use, ProSomnus devices have demonstrated excellent efficacy, safety, adherence, and overall outcomes in a growing body of clinical investigations. ProSomnus precision intraoral devices are FDA-cleared, patented, and covered by commercial medical insurance, Medicare, TRICARE and many Government sponsored healthcare plans around the world, representing over 200 million covered lives. To learn more, visit www.ProSomnus.com.
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