Alkermes Granted Orphan Drug Designations for Alixorexton in US, Europe
The investigational oral orexin 2 receptor agonist received designations from the FDA for idiopathic hypersomnia and the European Commission for narcolepsy.
The investigational oral orexin 2 receptor agonist received designations from the FDA for idiopathic hypersomnia and the European Commission for narcolepsy.
New research identifies a "strong response endotype" of patients who experience nearly double the sleep apnea improvement from tirzepatide.
In this one-hour webinar, sleep physician-presenters explore how to better identify, assess, and manage residual EDS in 2026—moving beyond the AHI to focus on real-world functional outcomes, patient-reported symptoms, and emerging treatment strategies.
The shift to home sleep testing is forcing a rethink of how respiratory effort is captured, validated, and clinically applied.
Research using contactless at-home monitoring over eight weeks reveals a hallmark difference that distinguishes chronic insomnia patients from those without the condition.
The REVITALYZ study met its primary endpoint, demonstrating significant improvements in excessive daytime sleepiness for adults with idiopathic hypersomnia treated with once-nightly LUMRYZ.
AesyBite Active demonstrated a statistically significant reduction in bruxism activity and improved orofacial pain in a study of 26 patients, supporting Aesyra’s push for FDA approval in 2026.
A new clinical trial from Mass General Brigham found that a drug approved for other indications helped early morning shift workers with shift work disorder stay more alert.
Yanchen Wang is named among 300 scholars in the Regeneron Science Talent Search 2026 for her project investigating the characteristics and risk factors of the parasomnia.