Northwire Canada EditionMonday, July 13, 2026
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GLDN 0.055 +0.0% BRON 0.040 +0.0% BTO 5.43 −0.7% ESK 0.365 −2.7% AUMN 0.275 +0.0% GGX 0.040 +0.0% S 0.155 +29.2% NNX 0.035 +0.0% ABX 51.90 −0.6% TTS 2.40 −4.0% FCI 0.400 −9.1% GR 0.075 +0.0% AII 23.38 +12.4% TUNG 1.72 +1.8% LGO 1.01 −2.9% EMM 0.080 +0.0% GLDN 0.055 +0.0% BRON 0.040 +0.0% BTO 5.43 −0.7% ESK 0.365 −2.7% AUMN 0.275 +0.0% GGX 0.040 +0.0% S 0.155 +29.2% NNX 0.035 +0.0% ABX 51.90 −0.6% TTS 2.40 −4.0% FCI 0.400 −9.1% GR 0.075 +0.0% AII 23.38 +12.4% TUNG 1.72 +1.8% LGO 1.01 −2.9% EMM 0.080 +0.0%
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Theralase(R) Discovers Further Mechanism on How Ruvidar(R) Inactivates Herpes Simplex Virus

TLT · Price

Executive Summary

  • Theralase® Technologies announced the identification of an additional mechanism of action (MOA) by which its antiviral candidate Ruvidar® (TLD‑1433) inactivates Herpes Simplex Virus‑1 (HSV‑1).
  • The new MOA involves electrostatic attraction: positively charged Ruvidar® binds to negatively charged HSV‑1, neutralizing the virus surface charge and preventing cell entry.
  • In vitro studies showed complete viral destruction at micromolar concentrations (1.3 µM), achieving up to an 8‑log (99.999999 %) reduction in viable virions.

Key Details

  • Study Design: Pre‑clinical in‑vitro experiments measuring zeta potential to assess electrostatic binding between Ruvidar® and HSV‑1, followed by viral infectivity assays.
  • Electrostatic MOA Evidence:
  • Zeta potential measurements demonstrated a significant shift when Ruvidar® was combined with HSV‑1, confirming charge neutralization.
  • Figure 2 (binding assay) illustrates the reduction of negative surface charge on HSV‑1 after exposure to Ruvidar®.
  • Viral Inactivation Results:
  • At 1,300 nM (1.3 µM), Ruvidar® achieved complete HSV‑1 inactivation, delivering up to an 8‑log reduction in viral load (99.999999 % kill).
  • Figure 3 displays the dose‑response curve confirming this potency.
  • Comparative Efficacy: Prior data (April 10 2025 & September 24 2025) showed Ruvidar® superior to Acyclovir; the new MOA adds a third antiviral pathway.
  • Implications for Development:
  • The additional MOA supports continued pre‑clinical and planned clinical development of a topical HSV‑1 treatment slated to commence in 2026.
  • Enhances the therapeutic rationale for Ruvidar® as a multi‑modal antiviral agent targeting virus entry, replication, and intracellular survival.
  • Quotes:
  • Pavel Kaspler, PhD (Research Scientist): “This latest preclinical study has demonstrated that Ruvidar® is very effective in inactivating HSV‑1 by binding to the virus and neutralizing its negative charge.”
  • Arkady Mandel, MD, PhD, DSc (Chief Scientific Officer): Emphasized the significance of the new MOA for billions affected by viral infections.
  • Roger DuMoulin‑White, B.Sc., P.Eng. (President & CEO): “Preclinical and clinical development for a topical HSV‑1 treatment is slated to commence in 2026.”

Notable Quotes

“Theralase®'s latest research offers valuable new insight into how Ruvidar® can help fight viral infections… we can now add to this list that Ruvidar® is able to bind to negatively charged components in the virus, preventing entry and replication.” – Arkady Mandel, MD, PhD, DSc


Materiality Assessment: Material – Positive (new scientifically substantiated MOA that materially advances the therapeutic profile of a lead product).

Read the original news release →

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