
Insights on Vibrance-2 Study Results of Alixorexton in Narcolepsy Type 2: Richard K. Bogan, MD, FCCP, FAASM
The associate clinical professor at the University of South Carolina School of Medicine discussed data presented at SLEEP 2026 from a phase 2 study of orexin 2 receptor agonist alixorexton in narcolepsy type 2. [WATCH TIME: 3 minutes]
WATCH TIME: 3 minutes | Captions are auto-generated and may contain errors.
"Orexin is the main neuropeptide. It’s the command-and-control center for wakefulness. Downstream regions of the brain respond to orexin to produce other monoaminergic amines that create state stability and keep us awake."
Alixorexton (Alkermes) is an investigational oral selective orexin 2 receptor agonist being evaluated for the treatment of narcolepsy type 1, narcolepsy type 2 (NT2), and idiopathic hypersomnia. Orexin is a neuropeptide produced in the lateral hypothalamus that plays a key role in regulating wakefulness through activation of multiple downstream wake-promoting pathways distributed throughout the brain. In new data from the phase 2 Vibrance-2 study (NCT06555783) presented at the
For context, Vibrance-2 was a phase 2, randomized, double-blind, placebo-controlled, dose-ranging trial that evaluated once-daily alixorexton at doses of 10 mg, 14 mg, or 18 mg vs placebo for 8 weeks in 93 patients with NT2. The study’s dual primary end points assessed changes from baseline to week 8 in mean sleep latency on the Maintenance of Wakefulness Test and changes from baseline to week 8 in Epworth Sleepiness Scale scores, comparing participants treated with alixorexton with those receiving placebo.
In an interview with NeurologyLive® at SLEEP 2026, sleep expert














