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Original Research Article

Clinical Efficacy and Safety of Donepezil on Cognitive and Global Function in Patients with Alzheimer’s Disease

A 24-Week, Multicenter, Double-Blind, Placebo-Controlled Study in Japan

Homma A.a · Takeda M.b · Imai Y.c · Udaka F.d · Hasegawa K.e · Kameyama M.d · Nishimura T.f

Author affiliations

aTokyo Metropolitan Institute of Gerontology, Tokyo, bOsaka University Graduate School of Medicine, Osaka, cSt. Marianna University School of Medicine, Toyoko Hospital, Kanagawa, dSumitomo Hospital, Osaka, eSt. Marianna University School of Medicine, Kanagawa, fKoshien University, Hyogo, Japan

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Dement Geriatr Cogn Disord 2000;11:299–313

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Article / Publication Details

First-Page Preview
Abstract of Original Research Article

Published online: October 20, 2000
Issue release date: November – December

Number of Print Pages: 15
Number of Figures: 5
Number of Tables: 6

ISSN: 1420-8008 (Print)
eISSN: 1421-9824 (Online)

For additional information: https://www.karger.com/DEM

Abstract

This study evaluated efficacy and safety of donepezil hydrochloride (donepezil) at 5 mg/day in patients with mild to moderately severe Alzheimer’s disease for 24 weeks in a double-blind, placebo-controlled comparative trial. In this study, 268 patients were enrolled and 39 of these (15%) were withdrawn. In the evaluable population of efficacy, Protocol-Compatible (PC) analyzed patients (n = 228), better effects than that of placebo were confirmed using two primary efficacy measures: a cognitive performance test, the Japanese version of the Alzheimer’s Disease Assessment Scale – cognitive subscale (ADAS-J cog, p = 0.003) and a clinical global assessment, the Japanese version of the Clinical Global Impression of Change (J-CGIC, p = 0.000). The superiority of donepezil was also shown by secondary measures: the Sum of the Boxes of the Clinical Dementia Rating (CDR-SB), the Mental Function Impairment Scale (MENFIS) and the caregiver-rated modified Crichton scale (CMCS). The same results were obtained in the intention-to-treat (ITT) analysis (n = 263). The incidence of drug-related adverse events was 10% (14/136) in the donepezil and 8% (10/131) in the placebo group; no significant difference was seen between the two groups. The main adverse events were gastrointestinal symptoms, and these were almost all mild, and they all disappeared with continued administration or temporary discontinuation of donepezil. These results indicate that the donepezil appears to be effective and well tolerated in patients with mild to moderately severe Alzheimer’s disease.

© 2000 S. Karger AG, Basel


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Article / Publication Details

First-Page Preview
Abstract of Original Research Article

Published online: October 20, 2000
Issue release date: November – December

Number of Print Pages: 15
Number of Figures: 5
Number of Tables: 6

ISSN: 1420-8008 (Print)
eISSN: 1421-9824 (Online)

For additional information: https://www.karger.com/DEM


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