drugset / Trial / NCT01309763

Safety and Tolerability of AFFITOPE AD03

NCT01309763 ↗

Phase 1 Completed 28 enrolled Affiris AG
RandomizedParallel-groupSingle-blindTreatment

Summary

This is a randomized, controlled, parallel group, patient-blinded, single-center, phase I pilot study to assess tolerability and safety of repeated subcutaneous administration of a single-dose of AFFITOPE AD03 applied with or without adjuvant to patients with mild to moderate Alzheimer's disease.

Timeline

Start
2010-10
Primary completion
2011-09
Completion
2011-11

Drugs

EvaluationDrugModalityDoseRoute
Comparator AFFITOPE AD03 Unknown — Subcutaneous
Background Alum Unknown — Subcutaneous

Indications