Health Canada Approves Zepbound for OSA in Adults With Obesity
Tirzepatide injection becomes the first medication authorized in Canada for moderate to severe OSA, demonstrating significant reductions in breathing disruptions in clinical trials.
Tirzepatide injection becomes the first medication authorized in Canada for moderate to severe OSA, demonstrating significant reductions in breathing disruptions in clinical trials.
The peer-reviewed study highlights how the sublingual cyclobenzaprine formulation targets nonrestorative sleep and bypasses first-pass metabolism.
The treatment was previously approved for excessive daytime sleepiness in pediatric patients 6 years of age and older with narcolepsy.
With the acquisition of Avadel Pharmaceuticals complete, Alkermes prepares to initiate phase 3 studies for its orexin agonist alixorexton while planning a leadership transition for mid-2026.
Read MoreThe low-sodium oxybate oral solution generated $1.7 billion in revenue, contributing to the company’s $3.1 billion neuroscience portfolio performance in 2025.
Read MoreThe CLARITY trial utilizes a randomized withdrawal design to assess time to relapse of depressive symptoms in patients with major depressive disorder and excessive daytime sleepiness.
Read MoreThe acquisition accelerates Alkermes’ entry into the sleep medicine market and incorporates the FDA-approved extended-release sodium oxybate treatment for narcolepsy.
Read MoreThe approval allows Amneal to offer a generic alternative for the treatment of cataplexy and excessive daytime sleepiness in narcolepsy patients, expanding access to this standard of care therapy.
Read MoreNew research suggests the orexin receptor antagonist prevents harmful protein buildup in the brain.
Read MoreThe company’s narcolepsy treatment shows strong growth, while its late-stage pipeline advances with five phase 3 trials and a novel orexin agonist.
Read MoreThe deal will bring the narcolepsy treatment LUMRYZ under the Alkermes portfolio.
Read MoreNew modeling from the University of Southern California suggests avoiding prescription sleep drugs could lower fall risk and cognitive impairment while increasing life expectancy.
Read MoreA new analysis of phase 3 trial data published in Maturitas supports the efficacy and safety of the dual orexin receptor antagonist for insomnia in this patient population.
Read MoreThe dual orexin receptor antagonist was honored as the ‘Best Biotechnology & Pharmaceutical Product’ in Europe-Middle East.
Read MoreThe increased offer values Avadel at up to approximately $2.37 billion.
Read MorePhase 4 DUET trial and real-world data presented at World Sleep 2025 and Psych Congress 2025 highlight low-sodium Xywav’s impact on sleep continuity, alertness, and cardiometabolic risk profiles in adults with narcolepsy or idiopathic hypersomnia.
Read MoreA study of nearly 1.8 million adults with diabetes suggests patients with obstructive sleep apnea derive a 20% greater mortality reduction from GLP-1 therapy than those without the sleep disorder.
Read MoreA retrospective study explores how surgical and pharmacologic weight-loss strategies stack up in cost, effectiveness, and health outcomes.
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