drugset / Trial / NCT00515333

TRx0014 in Patients With Mild or Moderate Alzheimer's Disease

NCT00515333

Phase 2 Completed 323 enrolled TauRx Therapeutics Ltd
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

EvaluationDrugModalityDoseRoute
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

Indications