CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 1,496 enrolled
Drug / intervention
Rosiglitazone Extended Release 2mg +3 moredrug
Likely dose
Rosiglitazone Extended Release 2mgfrom record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT00348309
NCT00348309N/ACompleted

A 54-week, Double-blind, Randomized, Placebo-controlled, Parallel-group Study to Investigate the Effects of Rosiglitazone (Extended Release Tablets) as Adjunctive Therapy to Donepezil on Cognition and Overall Clinical Response in APOE ε4-stratified Subjects With Mild to Moderate Alzheimer's Disease.

GlaxoSmithKline·interventional·Posted Jul 4, 2006·Updated Nov 28, 2017

In Brief

A clinical study evaluating Rosiglitazone Extended Release 2mg, Rosiglitazone Extended Release 8mg, and 2 other interventions for Alzheimer's Disease. Completed, enrolled 1,496 participants across 249 sites in 19 countries.

Detailed Summary

Rosiglitazone (RSG) has been tested in clinical studies and is approved by the FDA as a treatment for type II diabetes mellitus, a disease that occurs when the body is unable to effectively use glucose. RSG XR, the investigational drug used in this study, is an extended-release form of RSG. This study tests whether RSG XR safely provides clinical benefit to people with mild to moderate Alzheimer's disease (AD) when combined with the currently approved AD medication, Aricept (donepezil). RSG XR is a new approach to AD therapy and this study tests a new way to treat AD by testing whether one's genetic makeup affects their response to the study drug. Clinical data suggesting that RSG may benefit AD patients was first seen in a small study performed at the University of Washington and then from a larger GSK study conducted in Europe and New Zealand. In the first study, subjects receiving RSG once daily for 6 months scored significantly better on 3 tests of memory and thought than those who did not receive RSG. In the GSK study, those that appeared to benefit most from treatment with RSG XR had a specific genetic pattern. They did not have the gene that caused them to produce the protein apolipoprotein E e4 (APOE e4). Subjects who have the APOE e4 gene may have two copies, one from each parent, or they may have only one APOE e4 gene meaning that they inherited either the APOE e2 or APOE e3 version of the gene, instead of APOE e4, from one of their parents. Subjects with one copy of the APOE e4 gene remained at their same level of thinking ability while those with two copies of the APOE e4 gene, continued to worsen during the 6-month treatment. The current study will more directly test the effectiveness or RSG XR on people who either have or lack the APOE e4 gene.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesArgentina, Austria, Brazil, Canada, Chile, Czechia, France, Germany, Greece, Hungary, India, Italy, Japan, Mexico, Poland, Portugal, Spain, Switzerland, United States
Collaborators--

Timeline

N/ACompletedFinished
2006200720082009201020112012201320142015201620172018201920202021202220232024202520262027
First PostedJul 4, 2006
Enrollment StartJul 6, 2006
Primary CompletionJan 1, 2009
Study CompletionJan 28, 2009
TodayJul 2, 2026
Enrollment to primary: 2.5 yearsPosted 20.0 years ago

Interventions

Rosiglitazone Extended Release 2mgdrug

Rosiglitazone Extended Release 2mg OD

Rosiglitazone Extended Release 8mgdrug

Rosiglitazone Extended Release 8mg OD

Placeboother

Placebo

Donepezilother

Donepezil (At least 6 months of ongoing donepezil therapy for Alzheimer's disease, with stable dosing for at least the last 2 months (and with no intent to change for the duration of the study).