Last updated: 11/07/2018 01:15:45

Rosiglitazone (Extended Release Tablets) As Monotherapy In Subjects With Mild To Moderate Alzheimer’s Disease

GSK study ID
105640
Clinicaltrials.gov ID
EudraCT ID
EU CT Number
Not applicable
Trial status
Study complete
Study complete
Overview
Eligibility
Locations
Study documents
Results summary
Plain language summaries
Additional information

Trial overview

Official title: A 24-week, double-blind, double-dummy, randomized, parallel-group study to investigate the effects of rosiglitazone (extended release tablets), donepezil, and placebo as monotherapy on cognition and overall clinical response in APOE ε4-stratified subjects with mild to moderate Alzheimer’s disease. (REFLECT-1)
Trial description: Rosiglitazone (RSG) has been tested and is approved as a treatment for type II diabetes mellitus, a disease that occurs when the body ineffectively uses glucose. RSG XR, the investigational drug, is an extended-release form of RSG. This study tests whether RSG XR safely provides benefit to people with mild to moderate Alzheimer’s disease (AD). RSG XR is a new approach to AD therapy and this study tests whether one’s genes alter the effectiveness of RSG XR. Glucose is used by cells to make energy that they need to live. Changes in the ability of cells to use of glucose can lead to diseases like diabetes. Glucose levels may be lower in the brains of AD patients, and their brain cells may also use glucose less well than in unaffected people. The proper function of brain cells may be critical to memory and thought. If brain cells use glucose poorly, this might impact AD. Drugs that help brain cells properly use glucose may help a person maintain normal memory and thinking. Data suggesting that RSG may help AD patients was first seen in a small study at the Univ. of Washington and then from a larger international GSK study. In the first study, those receiving RSG once daily for 6 months scored better on 3 tests of memory and thought than those who did not receive RSG. In the GSK study, those that benefited most from therapy with RSG XR had a specific genetic pattern. They lacked the gene that caused them to produce 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 from one parent. Subjects with one copy of the APOE e4 gene remained fairly stable while those with two copies of APOE e4 continued to worsen during the 6-month treatment. This study will directly test the effect of RSG XR on people who either have or lack the APOE e4 gene.
Primary purpose:
Treatment
Trial design:
Parallel Assignment
Masking:
Double (Participant, Investigator)
Allocation:
Randomized
Primary outcomes:

Change from Baseline (W0) in mean ADAS-Cog total score at W24 as a function of APOE e4 status in Apolipoprotein epsilon4 (APOE e4) negative cohort

Timeframe: Baseline (W0) and W24

Change from Baseline (W0) in mean ADAS-Cog total score at W24 as a function of APOE e4 status in all except e4/e4’s cohort

Timeframe: Baseline (W0) and W24

Change from Baseline (W0) in mean ADAS-Cog total score at W24 as a function of APOE e4 status in full population cohort

Timeframe: Baseline (W0) and W24

Change from Baseline (W0) in mean CIBIC+ global functioning total score at W24 as a function of APOE e4 status in APOE4 negative cohort

Timeframe: Baseline (W0) and W24

Change from Baseline (W0) in mean CIBIC+ global functioning total score at W24 as a function of APOE e4 status in all except e4/e4’s cohort

Timeframe: Baseline (W0) and W24

Change from Baseline (W0) in mean CIBIC+ global functioning total score at W24 as a function of APOE e4 status in full population cohort

Timeframe: Baseline (W0) and W24

Secondary outcomes:

Change from Baseline (W0) in mean ADAS-Cog total score at W8, W16, W24

Timeframe: Baseline (W0) and up to W24

Change from Baseline (W0) in mean CIBIC+ global functioning total score at W8, W16, W24

Timeframe: Baseline (W0) and up to W24

Change from Baseline (W0) in mean Neuropsychiatric Inventory (NPI) total score at W8, W16, W24

Timeframe: Baseline (W0) and up to W24

Change from Baseline (W0) in mean Disability Assessment for Dementia (DAD) scale total score at W8, W16, W24

Timeframe: Baseline (W0) and up to W24

Change from Baseline (W0) in mean Short Term Memory Assessment total score (ADAS-Cog Q1 plus Q7) at W8, W16, W24

Timeframe: Baseline (W0) and up to W24

Change from Baseline (W0) in mean European Quality of Life -5 Dimensions Proxy version (EQ-5D Proxy) total score at W12, W24 assessed by utility

Timeframe: Baseline (W0) and up to W24

Change from Baseline (W0) in mean European Quality of Life -5 Dimensions Proxy version (EQ-5D Proxy) total score at W12, W24 assessed by Thermometer (visual analog scale [VAS])

Timeframe: Baseline (W0) and up to W24

Time spent caring for basic and instrumental activities Resource Utilization in Dementia (RUD) scale at W12 and W24

Timeframe: Baseline (W0) and up to W24

Change from Baseline (W0) in Alzheimer’s Carer’s Quality of Life Instrument (ACQLI) score at W12 and W24.

Timeframe: Baseline (W0) and up to W24

Change from Baseline (W0) in Mini Mental State Examination (MMSE) total score at W24.

Timeframe: Baseline (W0) and W24

Change from Baseline (W0) in glycosylated hemoglobin (HbA1c) at W24.

Timeframe: Baseline (W0) and W24

Number of participants with adverse events defined by severity

Timeframe: Up to W24

Number of participants with systolic and diastolic blood pressure (SBP and DBP), heart rate (HR) and weight values of potential clinical concern (PCC) any time on treatment (ATOT).

Timeframe: Up to W24

Change from Baseline (W0) in 12-lead Electrocardiogram (ECG)

Timeframe: Baseline (W0) and up to W24

Change from Baseline (W0) in heart rate (HR) measured from 12-lead Electrocardiogram (ECG)

Timeframe: Baseline (W0) and up to W24

Change from Baseline (W0) in body weight

Timeframe: Baseline (W0) and up to W24

Change from Baseline (W0) in hemoglobin

Timeframe: Baseline (W0) and up to W24

Change from Baseline (W0) in hematocrit

Timeframe: Baseline (W0) and Up to W24

Change from Baseline (W0) in periodic HbA1c assessment

Timeframe: Baseline (W0) and up to W24

Number of par. with hematology data of potential clinical concern any time on treatment

Timeframe: Up to W24

Number of par. with clinical chemistry values of potential clinical concern any time on treatment

Timeframe: Up to W24

Interventions:
  • Drug: Rosiglitazone
  • Enrollment:
    862
    Primary completion date:
    2008-05-09
    Observational study model:
    Not applicable
    Time perspective:
    Not applicable
    Clinical publications:
    Michael Gold, Claire Alderton, Marina Zvartau-Hind, Sally Egginton, Ann M Saunders, Michael Irizarry, Suzanne Craft, Gary Landreth, Ülla Linnamägi, Sharon Sawchak. Rosiglitazone Monotherapy in Mild-to-Moderate Alzheimer's Disease: Results from a Randomized, Double-Blind, Placebo-Controlled Phase 3 Study. Dement Geriatr Cogn Disord. 2010;30(2):131-46.
    Medical condition
    Alzheimer's Disease
    Product
    rosiglitazone
    Collaborators
    Not applicable
    Study date(s)
    February 2007 to September 2008
    Type
    Interventional
    Phase
    3

    Participation criteria

    Sex
    Female & Male
    Age
    50 - 90 years
    Accepts healthy volunteers
    No
    • Inclusion criteria:
    • Clinical diagnosis of probable Alzheimer’s Disease (AD).

    Trial location(s)

    Location
    Status
    Contact us
    Contact us
    Location
    GSK Investigational Site
    Memphis, Tennessee, United States, 35105
    Status
    Study Complete
    Location
    GSK Investigational Site
    West of Scotland Science Park, Glasgow, United Kingdom, G20 0XA
    Status
    Study Complete
    Location
    GSK Investigational Site
    Vienna, Austria, A-1130
    Status
    Terminated/Withdrawn
    Location
    GSK Investigational Site
    Moscow, Russia, 117049
    Status
    Study Complete
    Location
    GSK Investigational Site
    Kaposvár, Hungary, 7400
    Status
    Terminated/Withdrawn
    Location
    GSK Investigational Site
    Chemnitz, Sachsen, Germany, 09111
    Status
    Study Complete
    Showing 1 - 6 of 135 Results

    Study documents

    Clinical study report
    Available language(s): English
    Scientific result summary
    Available language(s): English

    If you wish to request for full study report, please contact - [email protected]

    Results overview

    Results posted on ClinicalTrials.gov

    Recruitment status
    Study complete
    Actual primary completion date
    2008-05-09
    Actual study completion date
    2008-05-09

    Plain language summaries

    Plain language summaries of clinical trial results for Phase 2-4 clinical trials that were initiated on or after January 2022 will be posted by GSK within one year following study completion.

    Additional information about the trial

    Participate in clinical trial
    Additional information
    Researchers can use this site to request access to anonymised patient level data and/or supporting documents from clinical studies to conduct further research.
    Click here
    Access to clinical trial data by researchers
    Visit website