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低钠羟丁酸钠在成年特发性发作性睡病患者3期临床研究开放标签滴定期的疗效与安全性

Efficacy and Safety of Lower-Sodium Oxybate in an Open-Label Titration Period of a Phase 3 Clinical Study in Adults with Idiopathic Hypersomnia.

作者信息

Thorpy Michael J, Arnulf Isabelle, Foldvary-Schaefer Nancy, Morse Anne Marie, Šonka Karel, Chandler Patricia, Hickey Luke, Chen Abby, Black Jed, Sterkel Amanda, Chen Dan, Bogan Richard K, Dauvilliers Yves

机构信息

Albert Einstein College of Medicine, Bronx, NY, USA.

Sleep Disorder Unit, Pitié-Salpêtrière Hospital and Sorbonne University, Paris, France.

出版信息

Nat Sci Sleep. 2022 Oct 26;14:1901-1917. doi: 10.2147/NSS.S369122. eCollection 2022.

Abstract

PURPOSE

To report the efficacy and safety of lower-sodium oxybate (LXB; Xywav) during the open-label titration and optimization period (OLT) and stable-dose period (SDP) in a clinical study for the treatment of idiopathic hypersomnia.

PATIENTS AND METHODS

Data were collected during treatment titration and optimization in a phase 3 randomized withdrawal trial in adults (18-75 years of age) with idiopathic hypersomnia who took LXB treatment (once, twice, or thrice nightly, administered orally) in the OLT (10-14 weeks), followed by the 2-week, open-label SDP. Endpoints included the Epworth Sleepiness Scale (ESS), Idiopathic Hypersomnia Severity Scale (IHSS), Patient Global Impression of Change, Clinical Global Impression of Change, Functional Outcomes of Sleep Questionnaire (FOSQ)-10, and Work Productivity and Activity Impairment Questionnaire: Specific Health Problem (WPAI:SHP).

RESULTS

The safety population included 154 participants; the modified intent-to-treat population comprised 115 participants. During open-label treatment, mean (SD) ESS scores improved (decreased) from 15.7 (3.8) at baseline to 6.1 (4.0) at end of SDP, and IHSS scores improved (decreased) from 31.6 (8.3) to 15.3 (8.5). Improvements were also observed during OLT in each individual IHSS item and in FOSQ-10 and WPAI:SHP scores. Thirty-five (22.7%) participants discontinued during OLT and SDP, 22 (14.3%) due to treatment-emergent adverse events (TEAEs) during OLT and SDP. The most frequent TEAEs in the first 4 weeks were nausea, headache, dizziness, and dry mouth; TEAE incidence decreased throughout OLT and SDP (weeks 1-4, n = 87 [56.5%]; weeks 13-16, n = 39 [31.7%]).

CONCLUSION

During open-label treatment with LXB, participants showed clinically meaningful improvements in idiopathic hypersomnia symptoms and in quality of life and functional measures. TEAE incidence declined over LXB titration and optimization.

摘要

目的

在一项治疗发作性睡病的临床研究中,报告低钠羟丁酸钠(LXB;Xywav)在开放标签滴定和优化期(OLT)以及稳定剂量期(SDP)的疗效和安全性。

患者与方法

在一项3期随机撤药试验中,收集了18至75岁患有发作性睡病的成人患者在治疗滴定和优化期间的数据,这些患者在OLT(10至14周)接受LXB治疗(每晚一次、两次或三次,口服给药),随后是为期2周的开放标签SDP。终点指标包括爱泼沃斯思睡量表(ESS)、发作性睡病严重程度量表(IHSS)、患者总体变化印象、临床总体变化印象、睡眠问卷功能结局(FOSQ)-10以及工作效率和活动障碍问卷:特定健康问题(WPAI:SHP)。

结果

安全人群包括154名参与者;改良意向性治疗人群包括115名参与者。在开放标签治疗期间,ESS平均(标准差)评分从基线时的15.7(3.8)改善(降低)至SDP结束时的6.1(4.0),IHSS评分从31.6(8.3)改善(降低)至15.3(8.5)。在OLT期间,每个IHSS单项以及FOSQ-10和WPAI:SHP评分也有改善。35名(22.7%)参与者在OLT和SDP期间停药,22名(14.3%)因OLT和SDP期间出现的治疗突发不良事件(TEAE)停药。前4周最常见的TEAE是恶心、头痛、头晕和口干;TEAE发生率在整个OLT和SDP期间下降(第1至4周,n = 87 [56.5%];第13至16周,n = 39 [31.7%])。

结论

在LXB的开放标签治疗期间,参与者在发作性睡病症状、生活质量和功能指标方面显示出具有临床意义的改善。TEAE发生率在LXB滴定和优化过程中下降。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7fb3/9618250/0612107b2945/NSS-14-1901-g0001.jpg

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