drugset / Trial / NCT00471211

Study Evaluating the Safety, Tolerability and Efficacy of PBT2 in Patients With Early Alzheimer's Disease

NCT00471211 ↗

Phase 2 Completed 80 enrolled Prana Biotechnology Limited
RandomizedParallel-groupDouble-blindTreatment

Summary

The purpose of the study is to determine the safety, tolerability and efficacy of 2 doses of PBT2 administered for 12 weeks compared to placebo in patients with early Alzheimer's disease treated with an acetylcholinesterase inhibitor.

Timeline

Start
2006-12
Primary completion
2007-12
Completion
2007-12

Drugs

EvaluationDrugModalityDoseRoute
Subject PBT2 Small molecule 50 mg —
Subject PBT2 Small molecule 250 mg —

Indications