drugset / Trial / NCT01230853

A Randomized, Double-blind, Placebo-controlled, Combined Single Ascending Dose and Multiple Ascending Dose Study

NCT01230853

Phase 1 Completed 80 enrolled Eisai Inc.
RandomizedSingle-groupQuadruple-blindTreatment

Summary

The purpose of this study will be to evaluate the safety and tolerability of lecanemab at sequentially ascending doses in subjects with mild to moderate Alzheimer's disease (AD).

Timeline

Start
2010-08
Primary completion
2012-10
Completion
2013-02

Drugs

EvaluationDrugModalityDoseRoute
Subject Lecanemab Monoclonal antibody 0.1 mg/kg Intravenous
Subject Lecanemab Monoclonal antibody 0.3 mg/kg Intravenous
Subject Lecanemab Monoclonal antibody 1 mg/kg Intravenous
Subject Lecanemab Monoclonal antibody 3 mg/kg Intravenous
Subject Lecanemab Monoclonal antibody 10 mg/kg Intravenous
Subject Lecanemab Monoclonal antibody 15 mg/kg Intravenous

Indications