drugset / Trial / NCT00495417

Tolerability and Safety of Subcutaneous Administration of Affitope AD01 in Mild to Moderate Alzheimer's Disease

NCT00495417 ↗

Phase 1 Completed 24 enrolled Affiris AG
RandomizedParallel-groupSingle-blindTreatment

Summary

The purpose of this study is to assess the tolerability and safety of repeated subcutaneous injection of a single dose of Affitope AD01 in patients with mild to moderate Alzheimer's Disease.

Timeline

Start
2007-07
Primary completion
2009-08
Completion
2009-08

Drugs

EvaluationDrugModalityDoseRoute
Comparator Affitope AD01 Unknown — Subcutaneous

Indications