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CNS Drugs. 2022 May;36(5):541-549. doi: 10.1007/s40263-022-00912-6. Epub 2022 Mar 31.
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.
钙、镁、钾和钠羟丁酸盐(Xywav;以下简称低钠羟丁酸盐)是一种新的羟丁酸盐制剂,与先前批准的钠羟丁酸盐(Xyrem)相比,其钠负荷大大降低。该药已被批准用于治疗伴有猝倒症和日间过度嗜睡(EDS)的成人和 7 岁及以上儿童的发作性睡病,也是美国批准用于治疗成人特发性嗜睡症的第一种药物。在两项关键性、双盲、安慰剂对照、随机撤药设计的 3 期临床试验中,低钠羟丁酸盐在开放标签滴定和优化期有效改善了伴有猝倒症和 EDS 的成年发作性睡病患者的猝倒症和 EDS,以及伴有 EDS 和整体特发性嗜睡症症状的成年特发性嗜睡症患者的 EDS 和整体特发性嗜睡症症状。在双盲、随机撤药期结束时,与继续接受低钠羟丁酸盐治疗的患者相比,随机转为安慰剂的患者在这些症状上出现了显著恶化。此外,与低钠羟丁酸盐相比,患者和临床评定的全球量表以及健康相关生活质量的衡量指标也出现了恶化。低钠羟丁酸盐总体上耐受性良好,其耐受性与钠羟丁酸盐大致相同。