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A 24-week double-blind placebo-controlled study of the efficacy and safety of the AMPA modulator S47445 in patients with mild to moderate Alzheimer's disease and depressive symptoms.
Bernard, Katy; Gouttefangeas, Sylvie; Bretin, Sylvie; Galtier, Stéphanie; Robert, Philippe; Holthoff-Detto, Vjera; Cummings, Jeffrey; Pueyo, Maria.
Afiliación
  • Bernard K; Institut de Recherches Internationales Servier (IRIS), Suresnes Cedex, France.
  • Gouttefangeas S; Institut de Recherches Internationales Servier (IRIS), Suresnes Cedex, France.
  • Bretin S; Institut de Recherches Internationales Servier (IRIS), Suresnes Cedex, France.
  • Galtier S; Institut de Recherches Internationales Servier (IRIS), Suresnes Cedex, France.
  • Robert P; CoBTeK IA lab, Memory Center, Université Côte d'azur, Nice, France.
  • Holthoff-Detto V; Alexianer Krankenhaus Hedwigshöhe, Berlin, Germany.
  • Cummings J; Department of Brain Sciences, Cleveland Clinic Lou Ruvo Center for Brain Health and University of Nevada Las Vegas, Las Vegas, NV, USA.
  • Pueyo M; Institut de Recherches Internationales Servier (IRIS), Suresnes Cedex, France.
Alzheimers Dement (N Y) ; 5: 231-240, 2019.
Article en En | MEDLINE | ID: mdl-31297437
INTRODUCTION: S47445 is a novel positive allosteric modulator of alpha-amino-3-hydroxy-5-methyl-4-isoxazole-propionic acid receptors that may emerge as a favorable candidate for the symptomatic treatment of cognitive and depressive disorders in patients suffering from Alzheimer's disease (AD) of mild to moderate severity and with depressive symptoms. METHODS: For this double-blind, placebo-controlled 24-week phase II trial, 520 outpatients aged between 55 and 85 years, with probable AD at mild to moderate stages (a Mini-Mental State Examination score of 24-15 inclusive) and exhibiting depressive symptoms (Cornell Scale for Depression in Dementia [CSDD] ≥ 8) were recruited in twelve countries and randomized to 3 doses of S47445 (5-15-50 mg) or placebo. The primary end point was the change from baseline in the 11-item Alzheimer's Disease Assessment Scale-Cognitive subscale (ADAS-Cog) total score at week 24. Secondary measures included the Disability Assessment for Dementia, Mini-Mental State Examination, ADAS-Cog 13-item, CSDD, Clinical Global Impression of Change (Alzheimer's Disease Cooperative Study-CGIC), Neuropsychiatric Inventory (NPI), and safety criteria. RESULTS: Baseline characteristics were comparable between the 4 groups. After 24 weeks, no statistically significant treatment difference was demonstrated between S47445 (5, 15 or 50 mg/d) and placebo on cognition (ADAS-Cog), function (Disability Assessment for Dementia), or depressive symptoms (CSDD). An improvement on neuropsychiatric symptoms assessed by NPI was evidenced at the lower dose 5 mg/d (Δ -2.55, P = .023, post hoc analysis) compared to placebo. CSDD and total NPI scores improved in all groups including placebo. There were no specific and/or unexpected safety signals observed with any of the S47445 doses. DISCUSSION: S47445 administered for 24 weeks was safe and well tolerated by patients with mild to moderate AD; the compound did not show significant benefits over placebo on cognition, function, or depressive symptoms.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Clinical_trials / Diagnostic_studies Idioma: En Revista: Alzheimers Dement (N Y) Año: 2019 Tipo del documento: Article País de afiliación: Francia Pais de publicación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Clinical_trials / Diagnostic_studies Idioma: En Revista: Alzheimers Dement (N Y) Año: 2019 Tipo del documento: Article País de afiliación: Francia Pais de publicación: Estados Unidos