drugset / Trial / NCT00411580

Safety and Tolerability Study in Patients With Mild to Moderate Alzheimer's Disease (AD)

NCT00411580

Phase 1 Completed 58 enrolled Novartis Pharmaceuticals
RandomizedParallel-groupQuadruple-blindTreatment

Summary

This study will evaluate the safety and tolerability and Aß-specific antibody response of CAD106 in patients with mild to moderate Alzheimer's Disease. Patients also had a 2 year follow-up to assess disease progression where no drug was administered.

Timeline

Start
2005-06
Primary completion
2008-12
Completion
2008-12

Drugs

EvaluationDrugModalityDoseRoute
Subject AMILOMOTIDE Protein / enzyme biologic 50 ug Subcutaneous
Subject AMILOMOTIDE Protein / enzyme biologic 150 ug Subcutaneous

Indications