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Study to Assess the Efficacy and Safety of MT-3921 in Subjects With Acute Traumatic Cervical Spinal Cord Injury

Spinal Cord Injury Clinical Trial

Official title:
A Phase 2a, Randomized, Double-blind, Placebo-controlled Study to Assess the Efficacy and Safety of MT-3921 in Subjects With Acute Traumatic Cervical Spinal Cord Injury

Clinical Trial Summary

The purpose of this study is to compare the efficacy and safety of intravenous (IV) infusions of MT-3921 to placebo in subjects with acute traumatic cervical spinal cord injury. Subjects meeting eligibility criteria will enter the 6-month double-blind period. Subjects will be randomized in a 2:1 ratio to receive MT-3921 or placebo in a double blind manner.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT04683848
Study type Interventional
Source Mitsubishi Tanabe Pharma America Inc.
Contact Clinical Trials Information Desk, to prevent miscommunication,
Phone please email:
Email information@mt-pharma-us.com
Status Recruiting
Phase Phase 2
Start date August 27, 2021
Completion date February 2025
View Details
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