Northwire Canada EditionThursday, October 15, 2026
Northwire
⌕
GOLD 4107.90 −1.7% SILVER 55.88 −6.1% COPPER 6.62 −1.6% OIL 95.09 +1.0% PALLADIUM 1096.50 −2.7% CIA 2.64 −0.4% BTO 7.09 −4.3% MCI 0.155 +0.0% CAN 0.065 +0.0% BLDS 0.335 +8.1% SAO 0.050 +0.0% SF 0.315 +0.0% BEA 0.055 −15.4% BMM 3.90 +11.1% AUGC 0.295 −13.2% MFG 3.34 −3.8% CDE 21.33 −7.7% CYG 0.160 −5.9% RSMX 0.100 −4.8% TUF 0.830 −5.7% GPG 0.285 −3.4% GOLD 4107.90 −1.7% SILVER 55.88 −6.1% COPPER 6.62 −1.6% OIL 95.09 +1.0% PALLADIUM 1096.50 −2.7% CIA 2.64 −0.4% BTO 7.09 −4.3% MCI 0.155 +0.0% CAN 0.065 +0.0% BLDS 0.335 +8.1% SAO 0.050 +0.0% SF 0.315 +0.0% BEA 0.055 −15.4% BMM 3.90 +11.1% AUGC 0.295 −13.2% MFG 3.34 −3.8% CDE 21.33 −7.7% CYG 0.160 −5.9% RSMX 0.100 −4.8% TUF 0.830 −5.7% GPG 0.285 −3.4%
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.