drugset / Trial / NCT00959192
Safety, Tolerability, And Immunogenicity Study Of ACC-001 In Japanese Subjects With Mild To Moderate Alzheimer's Disease
Phase 2
Completed
32 enrolled
Pfizer
JANSSEN Alzheimer Immunotherapy Research & Development, LLC · collab
RandomizedParallel-groupQuadruple-blindTreatment
Summary
The purpose of this study is to assess the safety, tolerability, and immunogenicity of ACC-001, an investigational vaccine, in subjects with mild to moderate Alzheimer's disease in Japan.
Timeline
- Start
- 2009-08
- Primary completion
- 2013-01
- Completion
- 2013-01
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Vanutide Cridificar | Vaccine | 3 ug | Intramuscular |
| Subject | Vanutide Cridificar | Vaccine | 10 ug | Intramuscular |
| Subject | Vanutide Cridificar | Vaccine | 30 ug | Intramuscular |