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A Study of Granexin® Gel for the Reduction of Scar Formation in Surgical Wounds Following Bilateral Anchor Incision Breast Surgery

Breast Reconstruction Clinical Trial

Official title:
A Phase 2b/3 Randomized, Prospective, Double Blind, Within-Subject Vehicle Controlled, Multi-Center Study to Determine the Efficacy and Safety of Granexin® Gel in Reducing Scar Formation in Surgical Wounds Following Bilateral Anchor Incision Breast Surgery

Clinical Trial Summary

The purpose of this study is to evaluate effectiveness of Granexin® gel in reducing scar formation in surgical incisional wounds.

Clinical Trial Description

Participants that meet screening criteria will be eligible for randomization providing all other criteria are met. Participants enrolled will receive study drug for 3 days. The participants will have an additional follow-up period to assess scarring of both Granexin® gel and Vehicle gel incisions through end of study at Month 12. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT04331080
Study type Interventional
Source Xequel Bio, Inc.
Contact
Status Completed
Phase Phase 2/Phase 3
Start date July 1, 2020
Completion date May 26, 2022
View Details
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