drugset / Trial / NCT01230853
A Randomized, Double-blind, Placebo-controlled, Combined Single Ascending Dose and Multiple Ascending Dose Study
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
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| 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 |