drugset / Trial / NCT00594737

Open Label Pilot Study of the Effects of Memantine on FDG-PET in Frontotemporal Dementia

NCT00594737

Phase 3 Completed 17 enrolled Tiffany Chow, MD H. Lundbeck A/S · collab
NaSingle-groupOpen-labelTreatment

Summary

Memantine has been approved for use in Alzheimer's disease. Its mechanism of action raises questions of whether it can also be effective for non-Alzheimer's dementias such as frontotemporal dementia (FTD), which currently has no disease-modifying treatment. This is an open-label study to probe the effects of memantine in 15 outpatients diagnosed with FTD, as shown objectively by comparing PET scans performed before and after use of the medication. The specific type of PET scan, FDG-PET, allows the investigators to gauge the effects of memantine on cortical activity levels. The investigators hypothesize that subjects on memantine will show normalization of cortical metabolic activity.

Timeline

Start
2007-10
Primary completion
2012-06
Completion
2012-06

Drugs

EvaluationDrugModalityDoseRoute
Subject Memantine Unknown 10 mg Oral