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Efficacy and Safety of Lower-Sodium Oxybate in an Open-Label Titration Period of a Phase 3 Clinical Study in Adults with Idiopathic Hypersomnia.
Thorpy, Michael J; Arnulf, Isabelle; Foldvary-Schaefer, Nancy; Morse, Anne Marie; Sonka, Karel; Chandler, Patricia; Hickey, Luke; Chen, Abby; Black, Jed; Sterkel, Amanda; Chen, Dan; Bogan, Richard K; Dauvilliers, Yves.
Afiliación
  • Thorpy MJ; Albert Einstein College of Medicine, Bronx, NY, USA.
  • Arnulf I; Sleep Disorder Unit, Pitié-Salpêtrière Hospital and Sorbonne University, Paris, France.
  • Foldvary-Schaefer N; Cleveland Clinic Sleep Disorders Center, Department of Neurology, Lerner College of Medicine, Cleveland, OH, USA.
  • Morse AM; Janet Weis Children's Hospital, Geisinger, Danville, PA, USA.
  • Sonka K; Department of Neurology, First Faculty of Medicine, Charles University and General University Hospital, Prague, Czech Republic.
  • Chandler P; Jazz Pharmaceuticals, Palo Alto, CA, USA.
  • Hickey L; Jazz Pharmaceuticals, Philadelphia, PA, USA.
  • Chen A; Jazz Pharmaceuticals, Palo Alto, CA, USA.
  • Black J; Jazz Pharmaceuticals, Palo Alto, CA, USA.
  • Sterkel A; Stanford University Center for Sleep Sciences and Medicine, Palo Alto, CA, USA.
  • Chen D; Jazz Pharmaceuticals, Palo Alto, CA, USA.
  • Bogan RK; Formerly Jazz Pharmaceuticals, Palo Alto, CA, USA.
  • Dauvilliers Y; University of South Carolina School of Medicine, Columbia, SC, USA.
Nat Sci Sleep ; 14: 1901-1917, 2022.
Article en En | MEDLINE | ID: mdl-36320423
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 (WPAISHP).

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 WPAISHP 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.
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Texto completo: 1 Base de datos: MEDLINE Tipo de estudio: Clinical_trials Idioma: En Revista: Nat Sci Sleep Año: 2022 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Base de datos: MEDLINE Tipo de estudio: Clinical_trials Idioma: En Revista: Nat Sci Sleep Año: 2022 Tipo del documento: Article País de afiliación: Estados Unidos