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Safety, pharmacokinetics, and pharmacodynamics of Gln-1062, a prodrug of galantamine.
Bakker, Charlotte; van der Aart, Jasper; Hart, Ellen P; Klaassen, Erica S; Bergmann, Kirsten R; van Esdonk, Michiel J; Kay, Denis G; Groeneveld, Geert Jan.
Afiliación
  • Bakker C; Centre for Human Drug Research Leiden The Netherlands.
  • van der Aart J; Centre for Human Drug Research Leiden The Netherlands.
  • Hart EP; Centre for Human Drug Research Leiden The Netherlands.
  • Klaassen ES; Centre for Human Drug Research Leiden The Netherlands.
  • Bergmann KR; Centre for Human Drug Research Leiden The Netherlands.
  • van Esdonk MJ; Centre for Human Drug Research Leiden The Netherlands.
  • Kay DG; Alpha Cognition Inc Vancouver BC Canada.
  • Groeneveld GJ; Centre for Human Drug Research Leiden The Netherlands.
Alzheimers Dement (N Y) ; 6(1): e12093, 2020.
Article en En | MEDLINE | ID: mdl-33083515
INTRODUCTION: Gln-1062 (MEMOGAIN) is an intranasally administered lipophilic prodrug of galantamine. Based on high brain-to-blood concentrations observed in pre-clinical studies, Gln-1062 is expected to have superior cognitive efficacy compared to oral galantamine. METHODS: Forty-eight healthy elderly subjects were randomized 12:4 to Gln-1062 (5.5, 11, or 22 mg, b.i.d., for 7 days) or placebo. Safety, tolerability, pharmacokinetics, and pharmacodynamics were assessed repeatedly. Pharmacokinetics were compared with 16 mg oral galantamine. RESULTS: Gln-1062 up to 22 mg, b.i.d., was well tolerated. Gln-1062 plasma concentrations increased immediately following dosing (median Tmax of 0.5 hour [range 0.5-1.0]). Cmax and AUC0-last increased in a dose-linear manner over all three dose levels. Gln-1062 was rapidly cleaved into galantamine. Gln-1062 significantly improved adaptive tracking (sustained attention) with 1.95% (95% confidence interval [CI] 0.630-3.279, P = 0.0055) compared to placebo after correction for individual baseline performance. DISCUSSION: Gln-1062 was considered to be safe and caused fewer gastrointestinal side effects than oral galantamine. Gln-1062 behaved pharmacokinetically as expected and improved performance on cognitive tests.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Clinical_trials Idioma: En Revista: Alzheimers Dement (N Y) Año: 2020 Tipo del documento: Article Pais de publicación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Clinical_trials Idioma: En Revista: Alzheimers Dement (N Y) Año: 2020 Tipo del documento: Article Pais de publicación: Estados Unidos