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Clinical Trial Summary

This combined phase 1/2a clinical trial is to investigate the safety, dose limiting toxicity (DLT), and exploratory efficacy of three repeated intraventricular administrations of NEUROSTEM® (human umbilical cord blood-derived mesenchymal stem cells) versus placebo via an Ommaya reservoir at 4 week intervals in patients with Alzheimer's disease.


Clinical Trial Description

The study is divided into the 2 stages: dose-escalation in stage 1 and randomized and multiple-dose cohort parallel design in stage 2.The target population for enrollment in this study is patients with mild to moderate Alzheimer's disease. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT02054208
Study type Interventional
Source Medipost Co Ltd.
Contact
Status Completed
Phase Phase 1/Phase 2
Start date March 2014
Completion date December 2019

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