Rosiglitazone (Extended Release Tablets) As Monotherapy In Subjects With Mild To Moderate Alzheimer’s Disease
Trial overview
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
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
- Inclusion criteria:
- Clinical diagnosis of probable Alzheimer’s Disease (AD).
- Inclusion criteria:
- Clinical diagnosis of probable Alzheimer’s Disease (AD).
- MMSE score 10 to 23
- Has not taken an approved AD therapy in last 30 days.
- No previous hypersensitivity/intolerance to AChEIs
- Have a regular caregiver. Exclusion criteria:
- Diagnosis of vascular dementia.
- Type I or secondary diabetes mellitus.
- Type II diabetes mellitus treated with insulin, sulfonylurea or glipizide.
- History or evidence of congestive heart failure, clinically significant peripheral edema or anemia.
- History of significant psychiatric illness, major depressive disorder or current depression needing initiation of treatment.
Trial location(s)
Study documents
If you wish to request for full study report, please contact - [email protected]
Results overview
Results posted on ClinicalTrials.gov
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.