A Study Evaluating Nexagon™ in the Treatment of Skin Wounds.

Status Completed

Clinical Trial Summary

Nexagon™ is a novel compound that promotes wound healing by temporarily disrupting cellular communication at the wound site, thereby promoting accelerated healing, reducing inflammation and pain. This randomized double-blind study will assess the safety, tolerability and clinical effect of Nexagon™ when applied to skin wounds created by punch biopsy in healthy volunteers. 43 healthy, fair-skinned males and females between ages 18-40 will be enrolled. Subjects will be reviewed again at 3 months and 9 months for follow-up safety assessments and wound appearance evaluation.

Clinical Trial Description

n/a

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Double Blind (Subject, Investigator, Outcomes Assessor), Primary Purpose: Treatment

Related Conditions & MeSH terms

Wound Healing

Clinical Trial Details

NCT number	NCT00736593
Study type	Interventional
Source	CoDa Therapeutics Inc.
Contact
Status	Completed
Phase	Phase 1
Start date	September 2008
Completion date	April 2009

View Details

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