Dose Escalation Study of AST-OPC1 in Spinal Cord Injury

Status Completed

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

Clinical Trial Details

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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