drugset / Trial / NCT00153010

An Evaluation of Three Doses of NS 2330 in Patients With Mild to Moderate Dementia of the Alzheimer's Type

NCT00153010

Phase 2 Completed 430 enrolled Boehringer Ingelheim
RandomizedParallel-groupDouble-blindTreatment

Summary

Objectives: The objective of this study will be to determine the safety, tolerability, drug blood levels, and efficacy of each of three doses of NS 2330 (Tesofensine) given once daily compared with placebo in patients with mild to moderate Dementia of the Alzheimer's Type.

Timeline

Start
2003-02
Primary completion
2005-03
Completion

Drugs

EvaluationDrugModalityDoseRoute
Subject Tesofensine Small molecule

Indications