drugset / Trial / NCT01297218

The Safety and The Efficacy Evaluation of NEUROSTEM®-AD in Patients With Alzheimer's Disease

NCT01297218 ↗

Phase 1 Completed 9 enrolled Medipost Co Ltd.
NaSingle-groupOpen-labelTreatment

Summary

The primary purpose of this study is to evaluate the safety and the tolerability of NEUROSTEM®-AD (Human Umbilical Cord Blood Derived Mesenchymal Stem Cells) and to assess the maximum tolerated dose (MTD). This study is also to investigate the efficacy of this study drug in patients with dementia of Alzheimer's type.

Timeline

Start
2011-02
Primary completion
2011-09
Completion
2011-12

Drugs

EvaluationDrugModalityDoseRoute
Subject human umbilical cord blood derived mesenchymal stem cells Cell therapy 3e+06 cells Other
Subject human umbilical cord blood derived mesenchymal stem cells Cell therapy 6e+06 cells Other

Indications