Axsome Advances Sleep Disorder Pipeline as Sunosi Prescriptions Increase in Q3
Q3 results highlight increased Sunosi prescriptions and advancements in Axsome’s late-stage trials for narcolepsy and shift work disorder.
Q3 results highlight increased Sunosi prescriptions and advancements in Axsome’s late-stage trials for narcolepsy and shift work disorder.
The company highlighted recently reported phase 3 results for AXS-12 in narcolepsy treatment, alongside revenue growth for Sunosi.
In a study comparing the effectiveness of wakefulness-promoting agents, researchers pinpointed which drug is likely the most effective in treating excessive daytime sleepiness for people with sleep apnea.
Read MoreAxsome Therapeutics reported first-quarter corporate updates, noting a growing patient base for Sunosi and progress for its narcolepsy drug candidate AXS-12.
Read MoreAccording to a review of 14 trials involving patients with OSA already on conventional therapy, adverse events associated with several wakefulness drugs increased the risk of discontinuation in several trials.
Read MoreSolriamfetol is being trialed in 59 patients with excessive daytime sleepiness associated with obstructive sleep apnea and impaired cognitive function.
Read MoreThe license agreement will expand the availability of Sunosi, a medicine used to reduce excessive daytime sleepiness in adults with narcolepsy or OSA, across Europe and MENA.
Read MoreNew research looked at whether a history of depression changed outcomes in patients with sleep apnea or narcolepsy who use solriamfetol to control excessive daytime sleepiness.
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