Northwire Canada EditionTuesday, August 25, 2026
Northwire
GOLD 4697.80 +0.4% SILVER 68.59 −1.4% COPPER 6.61 +0.3% OIL 85.01 −2.4% PALLADIUM 1359.75 +0.7% NVO 0.070 +0.0% SRA 0.780 +0.0% TUK 0.020 −20.0% GWM 0.610 −4.7% MINE 0.110 +0.0% EGM 0.100 +0.0% IRO 1.11 +2.8% CBR 1.41 +2.5% CTN 0.045 +0.0% GMX 2.06 +2.0% NPR 0.700 −2.8% CGD 1.28 +8.5% CRE 0.390 +13.0% PE 0.250 +0.0% PER 0.150 +7.1% SVRS 0.540 +8.0% GOLD 4697.80 +0.4% SILVER 68.59 −1.4% COPPER 6.61 +0.3% OIL 85.01 −2.4% PALLADIUM 1359.75 +0.7% NVO 0.070 +0.0% SRA 0.780 +0.0% TUK 0.020 −20.0% GWM 0.610 −4.7% MINE 0.110 +0.0% EGM 0.100 +0.0% IRO 1.11 +2.8% CBR 1.41 +2.5% CTN 0.045 +0.0% GMX 2.06 +2.0% NPR 0.700 −2.8% CGD 1.28 +8.5% CRE 0.390 +13.0% PE 0.250 +0.0% PER 0.150 +7.1% SVRS 0.540 +8.0%
Other

Devonian reports additional molecular data from MASH liver study

GSD · Price

Executive Summary

  • Devonian Health Group announced additional pre‑clinical gene expression results from its STAM™ mouse model of metabolic dysfunction‑associated steatohepatitis (MASH), confirming dose‑dependent anti‑inflammatory and anti‑fibrotic effects of Thykamine™.
  • At the highest tested dose (50 mg/kg), Thykamine™ markedly down‑regulated 29 fibrosis‑ and inflammation‑related genes, with several showing 80–90% reductions versus placebo.
  • The data provide molecular mechanistic support for previously reported histological improvements and will be included in a forthcoming scientific publication.

Key Details

  • Study Design: Oral Thykamine™ administered once daily for three weeks at 0.5 mg/kg, 5.0 mg/kg, and 50.0 mg/kg to STAM™ mice; placebo control group included.
  • Gene Panel: 29 genes examined – 13 fibrosis‑related, 5 inflammation‑related, 11 involved in both pathways.
  • Top Down‑regulated Fibrosis Genes (max dose): CCN1, CCN2, COL1A1, COL1A2, COL5A2, JAG1, MMP2, MMP13, SERPINE1, SERPINE2, SNAI1, TGFBR1.
  • Top Down‑regulated Inflammation Genes (max dose): CCL2, CCR2, IFNG, MMO8.
  • Dual‑role Genes Modulated: COL3A1, COL6A1, FN1, TGFB1, TIMP1, MMP14, TNF, IL10, TLR4.
  • Magnitude of Effect: Several genes exhibited 80–90% reduction relative to placebo at 50 mg/kg.
  • Dose‑Response: Consistent, progressive down‑regulation across low, mid, and high dose groups, indicating pharmacologic activity.
  • Regional Variation: Gene expression differed between caudal and lateral liver lobes, suggesting heterogeneous intra‑hepatic activity.
  • Analytical Methods: PCR performed by Dr. Louis Flamand (Université Laval); statistical analysis by Dr. John Sampalis (McGill University).
  • CEO Comment: “We are delighted to share these gene expression results… The data demonstrate that Thykamine™ modulates multiple genes involved in fibrosis and inflammation, reinforcing its potential to target underlying disease pathology and prevent progression of MASH.” – Dr. André P. Boulet, CEO.

Notable Quotes

  • “This study further adds to the growing body of evidence supporting Thykamine™'s multi‑targeting mode of action… results strengthen Thykamine™'s positioning across a broad array of inflammatory diseases, now including hepatic conditions alongside dermatology and Inflammatory Bowel Disease.” – Dr. André P. Boulet, CEO.
Read the original news release →

More from Devonian Health Group Inc.