International audienceStudy objectives: To assess the efficacy and safety of FT218, a novel once-nightly formulation of sodium oxybate (ON-SXB), in patients with narcolepsy in the phase 3 REST-ON trial.Methods: Narcolepsy patients aged ≥16 years were randomized 1:1 to uptitration of ON-SXB (4.5, 6, 7.5, and 9 g) or placebo. Three coprimary endpoints were change from baseline in mean sleep latency on the Maintenance of Wakefulness test, Clinical Global Impression-Improvement rating, and weekly cataplexy attacks at 9, 7.5, and 6 g. Secondary endpoints included change from baseline on the Epworth Sleepiness Scale. Safety included adverse drug reactions and clinical laboratory assessments.Results: In total, 222 patients were randomized; 212 rec...
Introduction: Sodium oxybate is indicated for the treatment of Excessive Daytime Sleepiness (EDS) an...
Introduction The present post hoc analysis was designed to evaluate health-related quality of life (...
Study Objectives: To evaluate adherence to sodium oxybate prescribing information for indication and...
International audienceStudy objectives: To assess the efficacy and safety of FT218, a novel once-nig...
BACKGROUND: Sodium oxybate has been recognized as a gold standard for the treatment of disrupted nig...
AbstractObjectiveThis study aimed to evaluate safety and efficacy of sodium oxybate (SXB) titrated t...
Introduction: Sodium oxybate is an effective treatment for excessive daytime sleepiness and cataplex...
Objective: This study aimed to evaluate safety and efficacy of sodium oxybate (SXB) titrated to effe...
Background: Narcolepsy is a lifelong neurological disorder with onset commonly in childhood or adole...
International audienceAbstract Study Objectives Evaluate efficacy and safety of lower-sodium oxybate...
Introduction: Sodium oxybate is indicated for the treatment of Excessive Daytime Sleepiness (EDS) an...
STUDY OBJECTIVES: Evaluate long-term efficacy and safety of sodium oxybate (SXB) in children and ado...
STUDY OBJECTIVES: This post hoc analysis evaluated the time to response that can be expected with so...
OBJECTIVE: To assess the effects of three narcolepsy treatment modalities on sleep stage shifts asso...
PurposeCurrent US FDA-approved treatments for narcolepsy include sodium oxybate (SXB) and calcium, m...
Introduction: Sodium oxybate is indicated for the treatment of Excessive Daytime Sleepiness (EDS) an...
Introduction The present post hoc analysis was designed to evaluate health-related quality of life (...
Study Objectives: To evaluate adherence to sodium oxybate prescribing information for indication and...
International audienceStudy objectives: To assess the efficacy and safety of FT218, a novel once-nig...
BACKGROUND: Sodium oxybate has been recognized as a gold standard for the treatment of disrupted nig...
AbstractObjectiveThis study aimed to evaluate safety and efficacy of sodium oxybate (SXB) titrated t...
Introduction: Sodium oxybate is an effective treatment for excessive daytime sleepiness and cataplex...
Objective: This study aimed to evaluate safety and efficacy of sodium oxybate (SXB) titrated to effe...
Background: Narcolepsy is a lifelong neurological disorder with onset commonly in childhood or adole...
International audienceAbstract Study Objectives Evaluate efficacy and safety of lower-sodium oxybate...
Introduction: Sodium oxybate is indicated for the treatment of Excessive Daytime Sleepiness (EDS) an...
STUDY OBJECTIVES: Evaluate long-term efficacy and safety of sodium oxybate (SXB) in children and ado...
STUDY OBJECTIVES: This post hoc analysis evaluated the time to response that can be expected with so...
OBJECTIVE: To assess the effects of three narcolepsy treatment modalities on sleep stage shifts asso...
PurposeCurrent US FDA-approved treatments for narcolepsy include sodium oxybate (SXB) and calcium, m...
Introduction: Sodium oxybate is indicated for the treatment of Excessive Daytime Sleepiness (EDS) an...
Introduction The present post hoc analysis was designed to evaluate health-related quality of life (...
Study Objectives: To evaluate adherence to sodium oxybate prescribing information for indication and...