Jazz Pharmaceuticals, Philadelphia, Pennsylvania.
Jazz Pharmaceuticals, Palo Alto, California.
J Clin Sleep Med. 2024 Sep 1;20(9):1467-1477. doi: 10.5664/jcsm.11182.
Low-sodium oxybate (LXB; calcium, magnesium, potassium, and sodium oxybates; Xywav) contains the same active moiety as high-sodium oxybates (SXBs; SXB [Xyrem] and fixed-dose SXB [Lumryz]), with 92% less sodium, and is approved in the United States for treatment of cataplexy or excessive daytime sleepiness in patients 7 years of age and older with narcolepsy, and idiopathic hypersomnia in adults. Patients with narcolepsy have increased cardiovascular risk relative to people without narcolepsy. LXB's lower sodium content is recognized by the United States Food and Drug Administration in the narcolepsy population as clinically meaningful in reducing cardiovascular morbidity compared with SXBs. The Substitution of Equal Grams of Uninterrupted Xyrem to Xywav study (NCT04794491) examined the transition experience of patients with narcolepsy switching from SXB to LXB.
Eligible participants were aged 18-80 years with narcolepsy type 1 or 2 on a stable SXB dose/regimen. After 2 weeks, participants transitioned gram-per-gram to LXB for 6 weeks, with opportunity for subsequent titration. Assessments included the Epworth Sleepiness Scale, Patient Global Impression of change, Ease of Switching Medication Scale, and Forced Preference Questionnaire.
The study enrolled 62 participants at baseline; 60 transitioned to LXB and 54 completed the study. At baseline and end of the LXB intervention/early discontinuation, respectively, mean total doses were 8.0 and 8.0 g/night; mean Epworth Sleepiness Scale scores were 9.4 and 8.8. Most participants reported improvement (45%) or no change (48%) in narcolepsy symptoms on the Patient Global Impression of change, reported the transition to LXB was "easy" (easy, extremely easy, not difficult at all; 93%) on the Ease of Switching Medication Scale, and preferred LXB compared with SXB (79%) on the Forced Preference Questionnaire, most commonly due to the lower sodium content.
Most participants switched from SXB to LXB with minimal modifications of dose/regimen and reported the transition process was easy. Effectiveness of oxybate treatment was maintained on LXB, and most participants preferred LXB to SXB. No new safety or tolerability issues were identified.
Registry: ClinicalTrials.gov; Name: An Interventional Safety Switch Study (Segue Study) of XYWAV in Narcolepsy; URL: https://classic.clinicaltrials.gov/ct2/show/NCT04794491; Identifier: NCT04794491.
Macfadden W, Leary EB, Fuller DS, Kirby MT, Roy A. Effectiveness and optimization of low-sodium oxybate in participants with narcolepsy switching from a high-sodium oxybate: data from the Substitution of Equal Grams of Uninterrupted Xyrem to Xywav study. . 2024;20(9):1467-1477.
低钠羟丁酸钠(LXB;钙、镁、钾和钠羟丁酸盐;Xywav)含有与高钠羟丁酸钠(SXBs;SXB [Xyrem]和固定剂量 SXB [Lumryz])相同的活性成分,但钠含量减少 92%,已获美国批准用于治疗 7 岁及以上患有嗜睡症的患者的猝倒或白天过度嗜睡,以及成人特发性嗜睡症。与没有嗜睡症的人相比,嗜睡症患者的心血管风险增加。美国食品和药物管理局认识到 LXB 的低钠含量在减少心血管发病率方面与 SXBs 相比具有临床意义,这在嗜睡症人群中得到认可。从 SXB 转换为 LXB 的等量连续 Xyrem 替代研究(NCT04794491)检查了从 SXB 转换为 LXB 的嗜睡症患者的转换体验。
符合条件的参与者年龄在 18-80 岁之间,患有 1 型或 2 型嗜睡症,正在服用稳定剂量的 SXB。2 周后,参与者按克数等量转换为 LXB,持续 6 周,随后有机会进行滴定。评估包括嗜睡量表、患者整体变化印象、药物转换容易程度量表和强制偏好问卷。
该研究在基线时招募了 62 名参与者;60 名参与者转为 LXB,54 名参与者完成了研究。在基线和 LXB 干预/早期停药时,平均总剂量分别为 8.0 和 8.0 g/夜;平均嗜睡量表评分分别为 9.4 和 8.8。大多数参与者报告嗜睡症症状改善(45%)或无变化(48%)(患者整体变化印象),报告药物转换到 LXB“容易”(容易、非常容易、一点也不难;93%)(药物转换容易程度量表),并在强制偏好问卷中更喜欢 LXB 而不是 SXB(79%),最常见的原因是钠含量较低。
大多数参与者以最小的剂量/方案调整从 SXB 转换为 LXB,并报告转换过程很容易。羟丁酸盐治疗的有效性在 LXB 上得到维持,大多数参与者更喜欢 LXB 而不是 SXB。没有发现新的安全性或耐受性问题。
Registry: ClinicalTrials.gov; 名称:Xywav 在嗜睡症中的安全切换干预研究(Segue 研究);URL: https://classic.clinicaltrials.gov/ct2/show/NCT04794491; 标识符:NCT04794491。
Macfadden W, Leary EB, Fuller DS, Kirby MT, Roy A. 嗜睡症患者从高钠羟丁酸钠转换为低钠羟丁酸钠后的有效性和优化:来自等量连续 Xyrem 替代 Xywav 研究的数据。睡眠医学杂志。2024;20(9):1467-1477.