Northwire Canada EditionTuesday, July 14, 2026
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W 0.500 +1.0% RDG 0.160 +0.0% ARIC 0.780 +4.0% VROY 3.44 +5.2% ROCK 3.81 +3.0% APMI 0.120 +0.0% EM 3.58 −4.8% ALS 66.04 +6.8% MEK 0.065 +44.4% TLO 6.00 +13.0% ADE 0.045 −66.7% FAIR 0.060 +33.3% SVRS 0.420 −2.3% RES 0.050 +42.9% CYG 0.120 +0.0% W 0.500 +1.0% RDG 0.160 +0.0% ARIC 0.780 +4.0% VROY 3.44 +5.2% ROCK 3.81 +3.0% APMI 0.120 +0.0% EM 3.58 −4.8% ALS 66.04 +6.8% MEK 0.065 +44.4% TLO 6.00 +13.0% ADE 0.045 −66.7% FAIR 0.060 +33.3% SVRS 0.420 −2.3% RES 0.050 +42.9% CYG 0.120 +0.0%
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Kane publishes article in International Wound Journal

KNE · Price

Executive Summary

  • Kane Biotech announced the publication of a peer-reviewed article in the International Wound Journal regarding its revyve anti-microbial wound gel.
  • The study validates the gel's thermo-reversible properties, demonstrating efficacy against broad-spectrum pathogens and sustained in vitro activity.
  • The publication serves as independent, peer-reviewed validation of the technology's safety and clinical potential, aimed at strengthening credibility with regulators and commercial partners.

Key Details

  • Publication Details: Article titled "Wound Healing Property of a Novel Thermo-Reversible Wound Gel With Lasting Antimicrobial and Antibiofilm Activity" published in the International Wound Journal.
  • Lead Author: Dr. Jeyachchandran Visvalingam (Internal R&D leader at Kane Biotech), with co-authors from the Miller School of Medicine, Dr. Phillip Frost Department of Dermatology and Cutaneous Surgery, University of Miami.
  • Product Mechanism: The thermo-reversible gel shifts from a low-viscosity liquid to a form-fitting gel at body temperature and reliquefies when cooled, allowing for easy, atraumatic removal.
  • Antimicrobial Efficacy: Demonstrated efficacy against a broad range of wound-related pathogens, specifically Staphylococcus aureus and Pseudomonas aeruginosa.
  • Bacterial Reduction: Achieved a 99.99% to 99.9999% reduction in bacterial counts within 30 minutes.
  • Sustained Activity: Showed sustained in vitro activity for up to seven days, which may potentially reduce the frequency of dressing changes.
  • Safety Validation: Safety and non-cytotoxicity were validated through biocompatibility testing and a porcine wound-healing study.
  • Regulatory Status: revyve anti-microbial wound gel is U.S. FDA 510(k)-cleared and Health Canada-approved.

Notable Quotes

  • "Having our research published in the International Wound Journal underscores the scientific rigour behind revyve technology and provides independent, peer-reviewed validation of the gel's safety, in vitro performance and clinical potential," said Dr. Robert Huizinga, interim chief executive officer. "Recognition in such a respected global wound-care publication strengthens our credibility with clinicians, regulators and commercial partners and reinforces our commitment to advancing evidence-based solutions that improve patient outcomes."
Read the original news release →

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