drugset / Trial / NCT00821561

A Study to Investigate the Safety and Clinical Effect of Nexagon® to Treat Persistent Epithelial Defects

NCT00821561 ↗

Phase 2 Withdrawn 90 enrolled OcuNexus Therapeutics, Inc.
RandomizedParallel-groupDouble-blindTreatment

Summary

The purpose of this study is to evaluate the efficacy and safety of Nexagon® in subjects with Persistent Epithelial Defects (PED) originally caused by chemical burns.

Timeline

Start
2009-03
Primary completion
2009-11
Completion
2010-03

Outcome

Outcome not reported

Stopped (Enrollment): “Withdrawn prior to recruitment for business reasons.”

Drugs

EvaluationDrugModalityDoseRoute
Subject CODA-001 Unknown — —

Indications