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Updated: Mar 12, 2026

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In Vitro Model of Human Cutaneous Hypertrophic Scarring using Macromolecular Crowding
Published on: May 1, 2020
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A Multicenter Randomized Controlled Trial Evaluating a Cx43-Mimetic Peptide in Cutaneous Scarring
Christina L Grek1, Jade Montgomery2, Meenakshi Sharma3
1FirstString Research, Inc., Mount Pleasant, South Carolina, USA.
The Journal of Investigative Dermatology
|November 19, 2016
Summary
The Cx43 mimetic peptide aCT1 significantly improved scar appearance in human incisional wounds 9 months post-surgery. This peptide formulation shows potential for reducing surgical scarring and enhancing wound healing outcomes.
Area of Science:
- Dermatology
- Wound Healing
- Regenerative Medicine
Background:
- Connexin 43 (Cx43) is a transmembrane protein involved in fibrotic processes, including inflammation and extracellular matrix regulation.
- Cx43 mimetic peptide aCT1 demonstrated preclinical efficacy in accelerating wound closure, reducing inflammation, and improving tissue mechanics.
- Surgical site scarring remains a significant concern, impacting both aesthetic and functional outcomes.
Purpose of the Study:
- To evaluate the efficacy and safety of aCT1 gel in reducing scar formation in human incisional wounds.
- To assess the long-term impact of aCT1 on scar appearance and characteristics.
Main Methods:
- A prospective, multicenter, within-participant controlled trial was conducted on patients with bilateral incisional wounds.
- Participants received either aCT1 gel plus standard care or standard care alone, applied acutely after surgery and 24 hours later.
- Scarring was assessed over 9 months using visual analog scales, Vancouver Scar Scale, and Global Assessment Scale.
Main Results:
- No significant difference in scar appearance was observed at 1 month post-treatment.
- At 9 months, aCT1-treated incisions showed a 47% improvement in scar scores (Vancouver Scar Scale) compared to controls (P=0.0045).
- Significant improvements were noted in Global Assessment Scale scores (P=0.0009), pigmentation, thickness, surface roughness, and mechanical suppleness.
Conclusions:
- aCT1 gel treatment significantly improves scar quality in human incisional wounds by 9 months post-surgery.
- The peptide demonstrated a favorable safety profile, with similar adverse events between treatment and control groups.
- aCT1 holds potential as a therapeutic agent to enhance surgical scarring outcomes.

