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Clinical Trial 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.


Clinical Trial Description

n/a


Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double-Blind, Primary Purpose: Treatment


Related Conditions & MeSH terms


NCT number NCT00821561
Study type Interventional
Source CoDa Therapeutics Inc.
Contact
Status Withdrawn
Phase Phase 2
Start date March 2009
Completion date March 2010

See also
  Status Clinical Trial Phase
Recruiting NCT03653650 - Autologous Platelet-rich Plasma in the Treatment of Persistent Epithelial Defects N/A