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Clinical Trial Summary

The purpose of this study is to evaluate the safety of cross sequential escalating doses of AST-OPC1 administered among 5 cohorts at a single time-point between 21 and 42 days post injury, inclusively, to subjects with subacute cervical spinal cord injuries (SCI).


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT02302157
Study type Interventional
Source Lineage Cell Therapeutics, Inc.
Contact
Status Completed
Phase Phase 1/Phase 2
Start date March 2015
Completion date December 2018

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