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Safety and Pharmacokinetics Study of MT-3921 in Spinal Cord Injury

2019-09-25 06:13:29 | BioPortfolio

Summary

The purpose of this study is to assess the safety, tolerability and pharmacokinetics of MT-3921 in subjects with spinal cord injury.

Description

This is a Phase 1, open-label, single ascending dose study of MT-3921 in subjects with spinal cord injury.

Study Design

Conditions

Spinal Cord Injury

Intervention

MT-3921 Low dose, MT-3921 High dose

Location

Barrow Neurological Institute/ St. Joseph's Hospital & Medical Center
Phoenix
Arizona
United States
85013

Status

Not yet recruiting

Source

Mitsubishi Tanabe Pharma Development America, Inc.

Results (where available)

View Results

Links

Published on BioPortfolio: 2019-09-25T06:13:29-0400

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