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.
A global survey reveals that peer connections significantly improve support and adjustment for individuals with narcolepsy and idiopathic hypersomnia.
Research has revealed potential clues into the pathophysiology of idiopathic hypersomnia.
New research has found that a sleep disorder thought to be rare may be as common as some other neurologic and psychiatric conditions such as epilepsy, bipolar disorder, and schizophrenia.
Read MoreThe Sleep Consortium, in collaboration with sleep-related patient advocacy organizations worldwide, has launched the Illuminate Hypersomnia initiative, an effort to highlight the lived experience of idiopathic hypersomnia.
Read MoreIn the third quarter, low-sodium Xywav grew 30% year-over-year, despite additional competition, with continued adoption across both narcolepsy and idiopathic hypersomnia
Read MoreIn its third-quarter business update, Zevra Therapeutics Inc designated KP1077, its investigational drug in development for idiopathic hypersomnia and narcolepsy, as a pivotal focus area.
Read MoreHarmony Biosciences reported a 37% increase in net revenue in the third quarter, largely attributed to the growth in patient use of its narcolepsy drug Wakix.
Read MoreJazz Pharmaceuticals announced new data highlighting the importance of low-sodium treatment options to help manage cardiovascular risk in patients with narcolepsy and idiopathic hypersomnia.
Read MoreAt World Sleep 2023, Jazz Pharmaceuticals will spotlight the link between sleep disorders and cardiovascular health through 14 abstracts.
Read MoreTopline results from the INTUNE study of pitolisant for idiopathic hypersomnia revealed that the primary endpoint for excessive daytime sleepiness did not achieve statistical significance against a placebo in the randomized withdrawal phase.
Read MoreInterim data from Zevra Therapeutics’ phase 2 clinical trial of KP1077 in patients with idiopathic hypersomnia indicates the drug is well-tolerated at all tested doses and dosing schedules.
Read MoreThe review evaluated all high-sodium oxybates, fixed-dose, and twice-nightly administrations in both oxybate-experienced patients and those who had not undergone prior treatment.
Read MoreZevra Therapeutics highlighted the heart safety of serdexmethylphenidate, the main ingredient in KP1077, its potential treatment for idiopathic hypersomnia, during a poster presentation at Psych Congress 2023.
Read MoreHarmony Biosciences is currently evaluating the efficacy and safety of pitolisant in adult patients with idiopathic hypersomnia in a phase 3 study, with topline results anticipated in the fourth quarter.
Read MoreFinancial assistance from The Assistance Fund is now available for eligible people living with idiopathic hypersomnia.
Read MoreNLS Pharmaceutics issued a letter updating stakeholders on its progress in developing treatments for sleep disorders, which include Mazindol ER for narcolepsy, NLS-4 for idiopathic hypersomnia, and NLS-11 for Kleine-Levin Syndrome.
Read MoreZevra Therapeutics provided second-quarter corporate updates, showcasing progress for KP1077, a drug candidate being investigated for the treatment of idiopathic hypersomnia and narcolepsy.
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