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Safety Study of GRNOPC1 in Spinal Cord Injury

Spinal Cord Injury Clinical Trial

Official title:
A Phase 1 Safety Study of GRNOPC1 in Patients With Neurologically Complete, Subacute, Spinal Cord Injury

Clinical Trial Summary

The purpose of the study is to evaluate the safety of GRNOPC1 administered at a single time-point between 7 and 14 days post injury, inclusive, to patients with neurologically complete spinal cord injuries (SCI).

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT01217008
Study type Interventional
Source Lineage Cell Therapeutics, Inc.
Contact
Status Completed
Phase Phase 1
Start date October 2010
Completion date July 2013
View Details
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