Study to Assess the Efficacy and Safety of VX-210 in Subjects With Acute Traumatic Cervical Spinal Cord Injury

Summary

The purpose of this study is to determine the efficacy and safety of VX-210 in subjects with Acute Traumatic Cervical Spinal Cord Injury. Secondary objectives include the specific evaluation of the effects of VX-210 on neurological recovery and daily function after spinal cord injury.

Timeline

Start

2016-07

Primary completion

2018-11

Completion

2018-11

Outcome

Missed primary endpoint

registry analysis (superiority test); Placebo vs VX-210 9 mg; p = 0.7519 NCT02669849 ↗

Drugs

Indications