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
Completed
Completed
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
Observational study model:
Not applicable
Primary completion date:
2008-05-09
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
  • Clinical diagnosis of probable Alzheimer’s Disease (AD).
  • MMSE score 10 to 23
  • Diagnosis of vascular dementia.
  • Type I or secondary diabetes mellitus.

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
Location
GSK Investigational Site
Tallinn, Estonia, 10614
Status
Study Complete
Location
GSK Investigational Site
Vienna, Austria, A-1090
Status
Study Complete
Location
GSK Investigational Site
Sunrise, Florida, United States, 33351
Status
Study Complete
Location
GSK Investigational Site
Toms River, New Jersey, United States, 08755
Status
Terminated/Withdrawn
Location
GSK Investigational Site
Deerfield Beach, Florida, United States, 33064
Status
Study Complete
Location
GSK Investigational Site
Nuernberg, Bayern, Germany, 90402
Status
Study Complete
Location
GSK Investigational Site
Leipzig, Sachsen, Germany, 04103
Status
Terminated/Withdrawn
Location
GSK Investigational Site
Phoenix, Arizona, United States, 85004
Status
Study Complete
Location
GSK Investigational Site
Berlin, Berlin, Germany, 12167
Status
Study Complete
Location
GSK Investigational Site
Halle, Sachsen-Anhalt, Germany, 06122
Status
Study Complete
Location
GSK Investigational Site
Guangzhou, Guangdong, China, 510370
Status
Study Complete
Location
GSK Investigational Site
Pécs, Hungary, 7623
Status
Study Complete
Location
GSK Investigational Site
Melbourne, Florida, United States, 32901
Status
Study Complete
Location
GSK Investigational Site
Tampa, Florida, United States, 33647
Status
Study Complete
Location
GSK Investigational Site
Toledo, Ohio, United States, 43623
Status
Study Complete
Location
GSK Investigational Site
Reseda, California, United States, 91355
Status
Study Complete
Location
GSK Investigational Site
Beijing, China, 100083
Status
Study Complete
Location
GSK Investigational Site
Ellwangen, Baden-Wuerttemberg, Germany, 73479
Status
Study Complete
Location
GSK Investigational Site
Koeln, Nordrhein-Westfalen, Germany, 50767
Status
Study Complete
Location
GSK Investigational Site
Atlanta, Georgia, United States, 30033
Status
Terminated/Withdrawn
Location
GSK Investigational Site
Hamburg, Hamburg, Germany, 22143
Status
Study Complete
Location
GSK Investigational Site
Hamburg, Hamburg, Germany, 20249
Status
Study Complete
Location
GSK Investigational Site
Plantation, Florida, United States, 33317
Status
Study Complete
Location
GSK Investigational Site
Ulm, Baden-Wuerttemberg, Germany, 89075
Status
Study Complete
Location
GSK Investigational Site
Centerville, Ohio, United States, 45459
Status
Study Complete
Location
GSK Investigational Site
St. Petersburg, Russia, 197022
Status
Study Complete
Location
GSK Investigational Site
San Juan, Puerto Rico, Puerto Rico, 00918
Status
Study Complete
Location
GSK Investigational Site
DeSoto, Texas, United States, 75115
Status
Study Complete
Location
GSK Investigational Site
Albany, New York, United States, 12208
Status
Study Complete
Location
GSK Investigational Site
Muenchen, Bayern, Germany, 80331
Status
Study Complete
Location
GSK Investigational Site
Destin, Florida, United States, 32541
Status
Study Complete
Location
GSK Investigational Site
San Diego, California, United States, 92120
Status
Study Complete
Location
GSK Investigational Site
Tartu, Estonia, 51014
Status
Study Complete
Location
GSK Investigational Site
Beijing, China, 100730
Status
Study Complete
Location
GSK Investigational Site
Oklahoma City, Oklahoma, United States, 73112
Status
Terminated/Withdrawn
Location
GSK Investigational Site
Philadelphia, Pennsylvania, United States, 19102
Status
Study Complete
Location
GSK Investigational Site
Muenchen, Bayern, Germany, 81675
Status
Terminated/Withdrawn
Location
GSK Investigational Site
Dresden, Sachsen, Germany, 01307
Status
Study Complete
Location
GSK Investigational Site
Providencia / Santiago, Región Metro De Santiago, Chile, 7500710
Status
Study Complete
Location
GSK Investigational Site
Nagpur, India, 440010
Status
Terminated/Withdrawn
Location
GSK Investigational Site
Santiago, Región Metro De Santiago, Chile, 7560356
Status
Study Complete
Location
GSK Investigational Site
Norwalk, Connecticut, United States, 06851
Status
Terminated/Withdrawn
Location
GSK Investigational Site
Las Vegas, Nevada, United States, 89146
Status
Study Complete
Location
GSK Investigational Site
Juelich, Nordrhein-Westfalen, Germany, 52428
Status
Study Complete
Location
GSK Investigational Site
Lahore, Pakistan, 54000
Status
Study Complete
Location
GSK Investigational Site
Itzehoe, Schleswig-Holstein, Germany, 25524
Status
Terminated/Withdrawn
Location
GSK Investigational Site
Unterhaching, Bayern, Germany, 82008
Status
Study Complete
Location
GSK Investigational Site
Linz, Austria, 4020
Status
Study Complete
Location
GSK Investigational Site
Pasig City, Philippines, 1600
Status
Study Complete
Location
GSK Investigational Site
Seoul, South Korea, 143-729
Status
Study Complete
Location
GSK Investigational Site
Tianjin, China, 300052
Status
Study Complete
Location
GSK Investigational Site
Karachi, Pakistan, 74800
Status
Study Complete
Location
GSK Investigational Site
Los Angeles, California, United States, 90036
Status
Terminated/Withdrawn
Location
GSK Investigational Site
Shanghai, China, 200025
Status
Study Complete
Location
GSK Investigational Site
Duisburg, Nordrhein-Westfalen, Germany, 47051
Status
Study Complete
Location
GSK Investigational Site
Middleton, Wisconsin, United States, 53562-2215
Status
Study Complete
Location
GSK Investigational Site
Hamburg, Hamburg, Germany, 22083
Status
Study Complete
Location
GSK Investigational Site
Lahore, Pakistan, 54590
Status
Study Complete
Location
GSK Investigational Site
Denver, Colorado, United States, 80218
Status
Terminated/Withdrawn
Location
GSK Investigational Site
San Francisco, California, United States, 94109
Status
Terminated/Withdrawn
Location
GSK Investigational Site
Sofia, Bulgaria, 1113
Status
Study Complete
Location
GSK Investigational Site
Kenilworth, New Jersey, United States, 07033
Status
Study Complete
Location
GSK Investigational Site
Viña del Mar, Valparaíso, Chile, 252-0997
Status
Study Complete
Location
GSK Investigational Site
Bochum, Nordrhein-Westfalen, Germany, 44892
Status
Study Complete
Location
GSK Investigational Site
Schwerin, Mecklenburg-Vorpommern, Germany, 19055
Status
Study Complete
Location
GSK Investigational Site
Szeged, Hungary, 6725
Status
Study Complete
Location
GSK Investigational Site
Fairfield, Connecticut, United States, 06824
Status
Terminated/Withdrawn
Location
GSK Investigational Site
Dubrovnik, Croatia, 20000
Status
Study Complete
Location
GSK Investigational Site
Cleveland, Ohio, United States, 44120
Status
Study Complete
Location
GSK Investigational Site
Cabo Rojo, Puerto Rico, Puerto Rico, 623
Status
Terminated/Withdrawn
Location
GSK Investigational Site
Bangalore, India, 560034
Status
Terminated/Withdrawn
Location
GSK Investigational Site
San Antonio, Texas, United States, 78229-3900
Status
Study Complete
Location
GSK Investigational Site
Puente Alto - Santiago, Región Metro De Santiago, Chile, 8207257
Status
Study Complete
Location
GSK Investigational Site
Mexico, Mexico, 14000
Status
Study Complete
Location
GSK Investigational Site
Berlin, Berlin, Germany, 13125
Status
Terminated/Withdrawn
Location
GSK Investigational Site
Hall in Tirol, Austria, A-6060
Status
Study Complete
Location
GSK Investigational Site
Saltillo, Coahuila, Mexico, 25000
Status
Study Complete
Location
GSK Investigational Site
Palo Alto, California, United States, 94305
Status
Study Complete
Location
GSK Investigational Site
St. Paul, Minnesota, United States, 55101
Status
Study Complete
Location
GSK Investigational Site
Jenkintown, Pennsylvania, United States, 19046
Status
Terminated/Withdrawn
Location
GSK Investigational Site
Shanghai, China, 200040
Status
Study Complete
Location
GSK Investigational Site
Plovdiv, Bulgaria, 4000
Status
Study Complete
Location
GSK Investigational Site
Ulm, Baden-Wuerttemberg, Germany, 89073
Status
Study Complete
Location
GSK Investigational Site
Berlin, Berlin, Germany, 12163
Status
Study Complete
Location
GSK Investigational Site
Philadelphia, Pennsylvania, United States, 19104
Status
Terminated/Withdrawn
Location
GSK Investigational Site
Nashville, Tennessee, United States, 37212
Status
Study Complete
Location
GSK Investigational Site
Dresden, Sachsen, Germany, 01097
Status
Study Complete
Location
GSK Investigational Site
Monterrey, Nuevo León, Mexico, 64660
Status
Study Complete
Location
GSK Investigational Site
Tulsa, Oklahoma, United States, 74104
Status
Study Complete
Location
GSK Investigational Site
Budapest, Hungary, 1106
Status
Terminated/Withdrawn
Location
GSK Investigational Site
Seongnam-si,, South Korea, 463-707
Status
Study Complete
Location
GSK Investigational Site
Syracuse, New York, United States, 13210
Status
Study Complete
Location
GSK Investigational Site
Newport Beach, California, United States, 92660
Status
Terminated/Withdrawn
Location
GSK Investigational Site
Sofia, Bulgaria, 1431
Status
Study Complete
Location
GSK Investigational Site
San Juan, Puerto Rico, Puerto Rico, 90660
Status
Study Complete
Location
GSK Investigational Site
Bradford, United Kingdom, BD3 0DQ
Status
Study Complete
Location
GSK Investigational Site
Zagreb, Croatia, 10000
Status
Study Complete
Location
GSK Investigational Site
Bielefeld, Nordrhein-Westfalen, Germany, 33647
Status
Study Complete
Location
GSK Investigational Site
Tallinn, Estonia, 10138
Status
Study Complete
Location
GSK Investigational Site
Thessaloniki, Greece, 57010
Status
Study Complete
Location
GSK Investigational Site
Achim, Niedersachsen, Germany, 28832
Status
Study Complete
Location
GSK Investigational Site
Quezon City, Philippines, 1102
Status
Terminated/Withdrawn
Location
GSK Investigational Site
St.-Petersburg, Russia, 198103
Status
Study Complete
Location
GSK Investigational Site
Guenzburg, Bayern, Germany, 89312
Status
Study Complete
Location
GSK Investigational Site
Schwerin, Mecklenburg-Vorpommern, Germany, 19053
Status
Study Complete
Location
GSK Investigational Site
Delray Beach, Florida, United States, 33445
Status
Study Complete
Location
GSK Investigational Site
Tallinn, Estonia, 10617
Status
Study Complete
Location
GSK Investigational Site
Athens, Greece, 115 21
Status
Study Complete
Location
GSK Investigational Site
Tirupati, India, 517507
Status
Terminated/Withdrawn
Location
GSK Investigational Site
Shanghai, China, 200030
Status
Study Complete
Location
GSK Investigational Site
Tuebingen, Baden-Wuerttemberg, Germany, 72076
Status
Study Complete
Location
GSK Investigational Site
Berlin, Berlin, Germany, 14163
Status
Terminated/Withdrawn
Location
GSK Investigational Site
Melissia, Greece, 151 27
Status
Study Complete
Location
GSK Investigational Site
Derriford, Plymouth, United Kingdom, PL6 8BX
Status
Terminated/Withdrawn
Location
GSK Investigational Site
Berlin, Berlin, Germany, 13507
Status
Study Complete
Location
GSK Investigational Site
Graz-Eggenberg, Austria, A-8020
Status
Study Complete
Location
GSK Investigational Site
Gera, Thueringen, Germany, 07551
Status
Study Complete
Location
GSK Investigational Site
Vienna, Austria, 1030
Status
Terminated/Withdrawn
Location
GSK Investigational Site
Lima, Peru, Lima 13
Status
Study Complete
Location
GSK Investigational Site
Cleveland, Ohio, United States, 44195
Status
Study Complete
Location
GSK Investigational Site
Baesweiler, Nordrhein-Westfalen, Germany, 52499
Status
Study Complete
Location
GSK Investigational Site
Moscow, Russia, 115522
Status
Study Complete
Location
GSK Investigational Site
Auckland, New Zealand, 0622
Status
Study Complete
Location
GSK Investigational Site
Hannover, Niedersachsen, Germany, 30559
Status
Study Complete
Location
GSK Investigational Site
Gyula, Hungary, 5700
Status
Study Complete
Location
GSK Investigational Site
Bad Homburg, Hessen, Germany, 61348
Status
Study Complete
Location
GSK Investigational Site
San Antonio, Texas, United States, 78229
Status
Terminated/Withdrawn
Location
GSK Investigational Site
Hialeah, Florida, United States, 33016
Status
Study Complete
Location
GSK Investigational Site
Oklahoma City, Oklahoma, United States, 73118
Status
Study Complete

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
Completed
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

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