The transmembrane
protein Cx43 has key roles in fibrogenic processes including inflammatory signaling and extracellular matrix composition. aCT1 is a
Cx43 mimetic
peptide that in preclinical studies accelerated
wound closure, decreased
inflammation and granulation tissue area, and normalized mechanical properties after cutaneous injury. We evaluated the efficacy and safety of aCT1 in the reduction of
scar formation in human incisional
wounds. In a prospective, multicenter, within-participant controlled trial, patients with bilateral incisional
wounds (≥10 mm) after laparoscopic surgery were randomized to receive acute treatment (immediately after wounding and 24 hours later) with an aCT1 gel formulation plus conventional standard of care protocols, involving moisture-retentive
occlusive dressing, or standard of care alone. The primary efficacy endpoint was average
scarring score using visual analog scales evaluating incision appearance and healing progress over 9 months. There was no significant difference in
scar appearance between aCT1- or control-treated incisions after 1 month. At month 9, aCT1-treated incisions showed a 47% improvement in
scar scores over controls (Vancouver
Scar Scale; P = 0.0045), a significantly higher Global Assessment Scale score (P = 0.0009), and improvements in
scar pigmentation, thickness, surface roughness, and mechanical suppleness. Adverse events were similar in both groups. aCT1 has potential to improve
scarring outcome after surgery.