drugset / Trial / NCT00515333
TRx0014 in Patients With Mild or Moderate Alzheimer's Disease
RandomizedParallel-groupQuadruple-blindTreatment
Summary
The primary objective of the study is to investigate the effects of oral TRx0014 at three doses (30, 60 and 100 mg tid) compared with placebo on cognitive ability in patients with mild or moderate dementia of the Alzheimer type. Cognitive ability will be measured by the Alzheimer's Disease Assessment Scale - cognitive subscale (ADAS-cog). The primary evaluation will be made at 24 weeks.
Timeline
- Start
- 2004-08
- Primary completion
- 2007-12
- Completion
- 2007-12
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Comparator | Methylene Blue | Diagnostic / imaging agent | 30 mg | Oral |
| Comparator | Methylene Blue | Diagnostic / imaging agent | 60 mg | Oral |
| Comparator | Methylene Blue | Diagnostic / imaging agent | 100 mg | Oral |