A 24-Week, Randomized, Double-Blind, Placebo-Controlled Study to Evaluate the Efficacy, Safety and Tolerability of the Rivastigmine Patch in Japanese Patients with Alzheimer’s Disease

Background: As of 2010, the rivastigmine patch was licensed for the treatment of Alzheimer’s disease (AD) in 64 countries. Methods: This 24-week, multicenter, randomized, double-blind, placebo-controlled study evaluated the efficacy, safety and tolerability of the 5-cm2 (9-mg loading dose; 4.6 mg/24...

Full description

Bibliographic Details
Main Authors: Yu Nakamura, Yukimichi Imai, Masahiro Shigeta, Ana Graf, Toru Shirahase, Hyosung Kim, Akifumi Fujii, Joji Mori, Akira Homma
Format: Article
Language:English
Published: Karger Publishers 2011-06-01
Series:Dementia and Geriatric Cognitive Disorders Extra
Subjects:
Online Access:http://www.karger.com/Article/FullText/328929
id doaj-752c75f6bfca4637bfe80e509795d760
record_format Article
spelling doaj-752c75f6bfca4637bfe80e509795d7602020-11-25T03:20:55ZengKarger PublishersDementia and Geriatric Cognitive Disorders Extra1664-54642011-06-011116317910.1159/000328929328929A 24-Week, Randomized, Double-Blind, Placebo-Controlled Study to Evaluate the Efficacy, Safety and Tolerability of the Rivastigmine Patch in Japanese Patients with Alzheimer’s DiseaseYu NakamuraYukimichi ImaiMasahiro ShigetaAna GrafToru ShirahaseHyosung KimAkifumi FujiiJoji MoriAkira HommaBackground: As of 2010, the rivastigmine patch was licensed for the treatment of Alzheimer’s disease (AD) in 64 countries. Methods: This 24-week, multicenter, randomized, double-blind, placebo-controlled study evaluated the efficacy, safety and tolerability of the 5-cm2 (9-mg loading dose; 4.6 mg/24 h delivery rate) and 10-cm2 (18-mg loading dose; 9.5 mg/24 h delivery rate) rivastigmine patch in Japanese patients with AD. Results: In the primary analysis population (intent-to-treat last observation carried forward) at week 24, delayed deterioration was seen with the 10-cm2 patch versus placebo on the Japanese version of the Alzheimer’s Disease Assessment Scale-cognitive subscale (ADAS-J cog; p = 0.005) and the Japanese version of the Clinician’s Interview-Based Impression of Change plus Caregiver Input (CIBIC plus-J; p = 0.067). Participants receiving the rivastigmine patch showed numerically less decline versus placebo at week 24 on the CIBIC plus-J, although this did not reach statistical significance. Statistical significance for the CIBIC plus-J was met following adjustment for body weight and baseline Mini-Mental State Examination score as dynamic allocation factors (p = 0.042) and on the Disability Assessment for Dementia (DAD; p = 0.024) and Mental Function Impairment (MENFIS; p = 0.016) subscales. Serious adverse events were rare and were consistent with the known safety profile of the rivastigmine patch. Conclusion: The rivastigmine patch has a favorable efficacy and tolerability profile in Japanese patients with AD.http://www.karger.com/Article/FullText/328929Alzheimerߣs diseaseCholinesterase inhibitorsJapaneseRandomized clinical trialRivastigmine
collection DOAJ
language English
format Article
sources DOAJ
author Yu Nakamura
Yukimichi Imai
Masahiro Shigeta
Ana Graf
Toru Shirahase
Hyosung Kim
Akifumi Fujii
Joji Mori
Akira Homma
spellingShingle Yu Nakamura
Yukimichi Imai
Masahiro Shigeta
Ana Graf
Toru Shirahase
Hyosung Kim
Akifumi Fujii
Joji Mori
Akira Homma
A 24-Week, Randomized, Double-Blind, Placebo-Controlled Study to Evaluate the Efficacy, Safety and Tolerability of the Rivastigmine Patch in Japanese Patients with Alzheimer’s Disease
Dementia and Geriatric Cognitive Disorders Extra
Alzheimerߣs disease
Cholinesterase inhibitors
Japanese
Randomized clinical trial
Rivastigmine
author_facet Yu Nakamura
Yukimichi Imai
Masahiro Shigeta
Ana Graf
Toru Shirahase
Hyosung Kim
Akifumi Fujii
Joji Mori
Akira Homma
author_sort Yu Nakamura
title A 24-Week, Randomized, Double-Blind, Placebo-Controlled Study to Evaluate the Efficacy, Safety and Tolerability of the Rivastigmine Patch in Japanese Patients with Alzheimer’s Disease
title_short A 24-Week, Randomized, Double-Blind, Placebo-Controlled Study to Evaluate the Efficacy, Safety and Tolerability of the Rivastigmine Patch in Japanese Patients with Alzheimer’s Disease
title_full A 24-Week, Randomized, Double-Blind, Placebo-Controlled Study to Evaluate the Efficacy, Safety and Tolerability of the Rivastigmine Patch in Japanese Patients with Alzheimer’s Disease
title_fullStr A 24-Week, Randomized, Double-Blind, Placebo-Controlled Study to Evaluate the Efficacy, Safety and Tolerability of the Rivastigmine Patch in Japanese Patients with Alzheimer’s Disease
title_full_unstemmed A 24-Week, Randomized, Double-Blind, Placebo-Controlled Study to Evaluate the Efficacy, Safety and Tolerability of the Rivastigmine Patch in Japanese Patients with Alzheimer’s Disease
title_sort 24-week, randomized, double-blind, placebo-controlled study to evaluate the efficacy, safety and tolerability of the rivastigmine patch in japanese patients with alzheimer’s disease
publisher Karger Publishers
series Dementia and Geriatric Cognitive Disorders Extra
issn 1664-5464
publishDate 2011-06-01
description Background: As of 2010, the rivastigmine patch was licensed for the treatment of Alzheimer’s disease (AD) in 64 countries. Methods: This 24-week, multicenter, randomized, double-blind, placebo-controlled study evaluated the efficacy, safety and tolerability of the 5-cm2 (9-mg loading dose; 4.6 mg/24 h delivery rate) and 10-cm2 (18-mg loading dose; 9.5 mg/24 h delivery rate) rivastigmine patch in Japanese patients with AD. Results: In the primary analysis population (intent-to-treat last observation carried forward) at week 24, delayed deterioration was seen with the 10-cm2 patch versus placebo on the Japanese version of the Alzheimer’s Disease Assessment Scale-cognitive subscale (ADAS-J cog; p = 0.005) and the Japanese version of the Clinician’s Interview-Based Impression of Change plus Caregiver Input (CIBIC plus-J; p = 0.067). Participants receiving the rivastigmine patch showed numerically less decline versus placebo at week 24 on the CIBIC plus-J, although this did not reach statistical significance. Statistical significance for the CIBIC plus-J was met following adjustment for body weight and baseline Mini-Mental State Examination score as dynamic allocation factors (p = 0.042) and on the Disability Assessment for Dementia (DAD; p = 0.024) and Mental Function Impairment (MENFIS; p = 0.016) subscales. Serious adverse events were rare and were consistent with the known safety profile of the rivastigmine patch. Conclusion: The rivastigmine patch has a favorable efficacy and tolerability profile in Japanese patients with AD.
topic Alzheimerߣs disease
Cholinesterase inhibitors
Japanese
Randomized clinical trial
Rivastigmine
url http://www.karger.com/Article/FullText/328929
work_keys_str_mv AT yunakamura a24weekrandomizeddoubleblindplacebocontrolledstudytoevaluatetheefficacysafetyandtolerabilityoftherivastigminepatchinjapanesepatientswithalzheimersdisease
AT yukimichiimai a24weekrandomizeddoubleblindplacebocontrolledstudytoevaluatetheefficacysafetyandtolerabilityoftherivastigminepatchinjapanesepatientswithalzheimersdisease
AT masahiroshigeta a24weekrandomizeddoubleblindplacebocontrolledstudytoevaluatetheefficacysafetyandtolerabilityoftherivastigminepatchinjapanesepatientswithalzheimersdisease
AT anagraf a24weekrandomizeddoubleblindplacebocontrolledstudytoevaluatetheefficacysafetyandtolerabilityoftherivastigminepatchinjapanesepatientswithalzheimersdisease
AT torushirahase a24weekrandomizeddoubleblindplacebocontrolledstudytoevaluatetheefficacysafetyandtolerabilityoftherivastigminepatchinjapanesepatientswithalzheimersdisease
AT hyosungkim a24weekrandomizeddoubleblindplacebocontrolledstudytoevaluatetheefficacysafetyandtolerabilityoftherivastigminepatchinjapanesepatientswithalzheimersdisease
AT akifumifujii a24weekrandomizeddoubleblindplacebocontrolledstudytoevaluatetheefficacysafetyandtolerabilityoftherivastigminepatchinjapanesepatientswithalzheimersdisease
AT jojimori a24weekrandomizeddoubleblindplacebocontrolledstudytoevaluatetheefficacysafetyandtolerabilityoftherivastigminepatchinjapanesepatientswithalzheimersdisease
AT akirahomma a24weekrandomizeddoubleblindplacebocontrolledstudytoevaluatetheefficacysafetyandtolerabilityoftherivastigminepatchinjapanesepatientswithalzheimersdisease
AT yunakamura 24weekrandomizeddoubleblindplacebocontrolledstudytoevaluatetheefficacysafetyandtolerabilityoftherivastigminepatchinjapanesepatientswithalzheimersdisease
AT yukimichiimai 24weekrandomizeddoubleblindplacebocontrolledstudytoevaluatetheefficacysafetyandtolerabilityoftherivastigminepatchinjapanesepatientswithalzheimersdisease
AT masahiroshigeta 24weekrandomizeddoubleblindplacebocontrolledstudytoevaluatetheefficacysafetyandtolerabilityoftherivastigminepatchinjapanesepatientswithalzheimersdisease
AT anagraf 24weekrandomizeddoubleblindplacebocontrolledstudytoevaluatetheefficacysafetyandtolerabilityoftherivastigminepatchinjapanesepatientswithalzheimersdisease
AT torushirahase 24weekrandomizeddoubleblindplacebocontrolledstudytoevaluatetheefficacysafetyandtolerabilityoftherivastigminepatchinjapanesepatientswithalzheimersdisease
AT hyosungkim 24weekrandomizeddoubleblindplacebocontrolledstudytoevaluatetheefficacysafetyandtolerabilityoftherivastigminepatchinjapanesepatientswithalzheimersdisease
AT akifumifujii 24weekrandomizeddoubleblindplacebocontrolledstudytoevaluatetheefficacysafetyandtolerabilityoftherivastigminepatchinjapanesepatientswithalzheimersdisease
AT jojimori 24weekrandomizeddoubleblindplacebocontrolledstudytoevaluatetheefficacysafetyandtolerabilityoftherivastigminepatchinjapanesepatientswithalzheimersdisease
AT akirahomma 24weekrandomizeddoubleblindplacebocontrolledstudytoevaluatetheefficacysafetyandtolerabilityoftherivastigminepatchinjapanesepatientswithalzheimersdisease
_version_ 1724615731080855552