Phase 4
Completed N=277
A Clinical Study Evaluating the Effects of Memantine on Brain Atrophy in Patients With Alzheimer's Disease
Source: ClinicalTrials.gov NCT00862940 ↗Enrolled (actual)
277
Serious AEs
13.4%
Results posted
Jun 2011
Primary outcomePrimary: Total Brain Atrophy Rate Estimated Using Brain Boundary Shift Integral (BBSI) — 15.24; 15.32 mL/year — p=0.9754
Summary
Pre-clinical studies have demonstrated that memantine can decrease the neuronal toxicity associated with excessive glutamate release and calcium overload in neurons. Previous studies have shown that memantine helps to treat the symptoms of Alzheimer's Disease (AD). In AD, the rate of brain tissue loss, or atrophy, is faster than in normal aging and this seems to go hand in hand with some of the symptoms of the disease. This suggests that memantine treatment in AD could provide both symptomatic improvement and neuro-protective effects. The purpose of this study was to show whether memantine, in addition to providing symptomatic benefits, can slow the rate of brain atrophy as assessed using magnetic resonance imaging (MRI) technology.
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Total Brain Atrophy Rate Estimated Using Brain Boundary Shift Integral (BBSI) |
15.24; 15.32 | 0.9754 |
| SECONDARY Changes in Total Hippocampal Volume (HCV) |
-218; -220 | 0.842 |
| SECONDARY Cognitive and Behavioural Outcomes: Controlled Oral Word Association Test (COWAT) Total Score |
0.78; -0.90 | 0.034 sig |
| SECONDARY Cognitive and Behavioural Outcomes: Mini Mental State Examination (MMSE) Total Score |
-0.50; -0.74 | 0.602 |
Eligibility Criteria
Inclusion Criteria
- Outpatients at least 50 years of age with a current diagnosis of probable AD of moderate severity (MMSE score between 12 and 20, inclusive) consistent with NINCDS-ADRDA criteria and MRI scans
- Patients must have had a knowledgeable and reliable caregiver to accompany them to all clinic visits during the study
- Patients were either on or off existing acetylcholinesterase inhibitor (AChEI) treatment provided that the treatment had been initiated >6 months prior to screening, had stabilised with respect to dose for >3 months, and remained fixed during the entire study. AChEI treatment could not be initiated or modified during the study
Exclusion Criteria
- The patient had evidence of clinically significant active disease (including recent myocardial infarction and uncompensated congestive heart failure [NYHA II-IV])
- The patient had evidence of any clinically significant neurodegenerative disease or neurological disorder other than AD
- The patient was contraindicated for MRI
Other protocol-defined inclusion and exclusion criteria applied.
Data sourced from ClinicalTrials.gov (NCT00862940). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication. Informational only — not medical advice.