drugset / Trial / NCT01068353
Safety and Tolerability of Etanercept in Alzheimer's Disease
Phase 2
Completed
41 enrolled
University of Southampton
Hampshire Hospitals NHS Foundation Trust · collabWyeth is now a wholly owned subsidiary of Pfizer · collab
RandomizedSingle-groupQuadruple-blindTreatment
Summary
The primary aim of the study is to determine the safety and tolerability of etanercept in subjects with Alzheimer's Disease. The effects of etanercept on cognitive, behavioural, functional and immunological outcomes will be examined as secondary aims.
Timeline
- Start
- 2011-01
- Primary completion
- 2013-12
- Completion
- —
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Etanercept | Protein / enzyme biologic | 50 mg | Subcutaneous |