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AC105 in Patients With Acute Traumatic Spinal Cord Injury — AC105  

Acute Spinal Cord Injury Clinical Trial

Official title:
A Phase 2 Double-blind, Randomized, Placebo-controlled Study to Determine the Safety, Tolerability and Potential Activity of AC105 Following a Regimen of 6 Doses Over 30 Hours in Patients With Acute Traumatic Spinal Cord Injury (SCI).

Clinical Trial Summary

The principal aim of this study was to establish the feasibility of rapid administration, safety, and tolerability of AC105 in patients with acute spinal cord injury.

Clinical Trial Description

To determine safety and tolerability of AC105 following a regimen of 6 intravenous doses over 30 hours in patients with acute non-penetrating traumatic spinal cord injury (SCI). ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT01750684
Study type Interventional
Source Acorda Therapeutics
Contact
Status Terminated
Phase Phase 2
Start date July 2013
Completion date May 2015
View Details
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