drugset / Trial / NCT01656525

A Multiple-dose Study of Gantenerumab in Japanese Alzheimer&Apos;s Disease Patients

NCT01656525

Phase 1 Completed 28 enrolled Chugai Pharmaceutical
RandomizedParallel-groupDouble-blindTreatment

Summary

Objective of this study is to evaluate the safety, tolerability, pharmacokinetics and preliminary pharmacodynamic effects of multiple doses of Gantenerumab in subject with mild to moderate AD.

Timeline

Start
2012-06
Primary completion
2014-03
Completion
2014-06

Drugs

EvaluationDrugModalityDoseRoute
Subject Gantenerumab Monoclonal antibody 75 mg Subcutaneous
Subject Gantenerumab Monoclonal antibody 105 mg Subcutaneous
Subject Gantenerumab Monoclonal antibody 225 mg Subcutaneous

Indications