drugset / Trial / NCT00821561
A Study to Investigate the Safety and Clinical Effect of Nexagon® to Treat Persistent Epithelial Defects
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Stopped (Enrollment): “Withdrawn prior to recruitment for business reasons.”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
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | CODA-001 | Unknown | — | — |