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A Randomized Phase 2 KINETIC Trial Evaluating SAGE-324/BIIB124 in Individuals with Essential Tremor.
Elble, Rodger J; Ondo, William G; Lyons, Kelly E; Qin, Min; Garafola, Svetlana; Hersh, Bonnie; Lieu, TinaMarie; Arkilo, Dimitrios; Chuang, Rosalind; Bankole, Kemi; Pahwa, Rajesh.
Afiliación
  • Elble RJ; Department of Neurology, Southern Illinois University School of Medicine, Springfield, Illinois, USA.
  • Ondo WG; Department of Neurology, Houston Methodist Hospital, Houston, Texas, USA.
  • Lyons KE; Department of Neurology, University of Kansas Medical Center, Kansas City, Kansas, USA.
  • Qin M; Sage Therapeutics, Inc, Cambridge, Massachusetts, USA.
  • Garafola S; Sage Therapeutics, Inc, Cambridge, Massachusetts, USA.
  • Hersh B; Biogen Inc., Cambridge, Massachusetts, USA.
  • Lieu T; Sage Therapeutics, Inc, Cambridge, Massachusetts, USA.
  • Arkilo D; Sage Therapeutics, Inc, Cambridge, Massachusetts, USA.
  • Chuang R; Biogen Inc., Cambridge, Massachusetts, USA.
  • Bankole K; Sage Therapeutics, Inc, Cambridge, Massachusetts, USA.
  • Pahwa R; Department of Neurology, University of Kansas Medical Center, Kansas City, Kansas, USA.
Mov Disord ; 39(4): 733-738, 2024 Apr.
Article en En | MEDLINE | ID: mdl-38357797
ABSTRACT

BACKGROUND:

SAGE-324/BIIB124 is an investigational positive allosteric modulator of GABAA receptors.

OBJECTIVE:

KINETIC (NCT04305275), a double-blind, randomized, placebo-controlled, phase 2 study, evaluated SAGE-324/BIIB124 in individuals with essential tremor (ET).

METHODS:

Individuals aged 18 to 80 years were randomly assigned 11 to orally receive 60 mg of SAGE-324/BIIB124 or placebo once daily for 28 days. The primary endpoint was change from baseline in The Essential Tremor Rating Assessment Scale-Performance Subscale (TETRAS-PS) Item 4 (upper-limb tremor) at day 29 with SAGE-324/BIIB124 versus placebo.

RESULTS:

Between May 2020 and February 2021, 69 U.S. participants were randomly assigned to receive SAGE-324/BIIB124 (n = 34) or placebo (n = 35). There was a significant reduction from baseline in TETRAS-PS Item 4 at day 29 with SAGE-324/BIIB124 versus placebo (least squares mean [standard error] -2.31 [0.401] vs. -1.24 [0.349], P = 0.0491). The most common treatment-emergent adverse events included somnolence, dizziness, fatigue, and balance disorder.

CONCLUSION:

These results support further development of SAGE-324/BIIB124 for potential ET treatment. © 2024 Sage Therapeutics, Inc and The Authors. Movement Disorders published by Wiley Periodicals LLC on behalf of International Parkinson and Movement Disorder Society.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Temblor Esencial Tipo de estudio: Clinical_trials Límite: Adolescent / Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Revista: Mov Disord Asunto de la revista: NEUROLOGIA Año: 2024 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Temblor Esencial Tipo de estudio: Clinical_trials Límite: Adolescent / Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Revista: Mov Disord Asunto de la revista: NEUROLOGIA Año: 2024 Tipo del documento: Article País de afiliación: Estados Unidos