drugset / Trial / NCT02053883

Cethrin in Acute Cervical Spinal Cord Injury

NCT02053883 ↗

Phase 2/3 Withdrawn BioAxone BioSciences, Inc.
RandomizedParallel-groupQuadruple-blindTreatment

Summary

This is a multicenter, randomized, double-blind, placebo-controlled Phase IIb/III study designed to evaluate the efficacy and safety of Cethrin as a treatment for acute cervical spinal cord injury. During the trial, high and low doses of Cethrin will be compared with placebo.

Timeline

Start
2015-07
Primary completion
2016-05
Completion
—

Outcome

Outcome not reported

Stopped: “Compound recently partnered with another company for continued development.”

Drugs

EvaluationDrugModalityDoseRoute
Subject Cethrin Protein / enzyme biologic — Other

Indications