Unknown

Dataset Information

0

Calcium, Magnesium, Potassium and Sodium Oxybates (Xywav®) in Sleep Disorders: A Profile of Its Use.


ABSTRACT: Calcium, magnesium, potassium and sodium oxybates (Xywav®; hereafter referred to as lower-sodium oxybate), a new oxybate formulation with a greatly reduced sodium burden compared with previously approved sodium oxybate (Xyrem®), is approved for the treatment of cataplexy and excessive daytime sleepiness (EDS) in adults and children aged ≥ 7 years with narcolepsy, and is the first drug approved for the treatment of idiopathic hypersomnia in adults in the USA. In two pivotal, double-blind, placebo-controlled, phase 3 trials of randomized-withdrawal design, lower-sodium oxybate effectively improved cataplexy and EDS in adults with narcolepsy, and EDS and overall idiopathic hypersomnia symptoms in adults with idiopathic hypersomnia during open-label titration and optimization periods. At the end of the double-blind, randomized withdrawal period, participants randomized to switch to placebo experienced significant worsening in these symptoms compared with those randomized to continue lower-sodium oxybate. Furthermore, worsening in patient- and clinical-rated global scales, as well as measures of health-related quality of life were also seen with placebo versus lower-sodium oxybate. Lower-sodium oxybate is generally well tolerated, with the tolerability profile being largely consistent to that seen with sodium oxybate.

SUBMITTER: Heo YA 

PROVIDER: S-EPMC9095545 | biostudies-literature | 2022 May

REPOSITORIES: biostudies-literature

altmetric image

Publications

Calcium, Magnesium, Potassium and Sodium Oxybates (Xywav<sup>®</sup>) in Sleep Disorders: A Profile of Its Use.

Heo Young-A YA  

CNS drugs 20220331 5


Calcium, magnesium, potassium and sodium oxybates (Xywav<sup>®</sup>; hereafter referred to as lower-sodium oxybate), a new oxybate formulation with a greatly reduced sodium burden compared with previously approved sodium oxybate (Xyrem<sup>®</sup>), is approved for the treatment of cataplexy and excessive daytime sleepiness (EDS) in adults and children aged ≥ 7 years with narcolepsy, and is the first drug approved for the treatment of idiopathic hypersomnia in adults in the USA. In two pivotal,  ...[more]

Similar Datasets

| S-EPMC8976528 | biostudies-literature
| S-EPMC7400604 | biostudies-literature
| S-EPMC10584168 | biostudies-literature
| S-EPMC2916845 | biostudies-literature
| S-EPMC3535175 | biostudies-literature
| S-EPMC7009523 | biostudies-literature
| S-EPMC1366808 | biostudies-literature
| S-EPMC4059135 | biostudies-literature
| S-EPMC6499034 | biostudies-literature
| S-EPMC7953213 | biostudies-literature