Northwire Canada EditionFriday, July 10, 2026
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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% OGN 3.45 +2.1% MSA 6.67 +3.7% SGZ 0.040 −11.1% GRSL 0.310 −3.1% 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% OGN 3.45 +2.1% MSA 6.67 +3.7% SGZ 0.040 −11.1% GRSL 0.310 −3.1%
Production / Operations

LIR Life Sciences Reports Positive Interim Preclinical Results from Comparative Animal Study of Novel CPP-Enabled Transdermal Delivery of GLP/GIP-Based Therapies

SKNY · Price

Executive Summary

  • LIR Life Sciences reported positive interim results from a comparative mouse study of a CPP‑enabled topical semaglutide formulation, showing reduced blood glucose after an oral glucose challenge versus untreated controls.
  • The topical formulation achieved glucose‑lowering effects comparable to injectable semaglutide, marking a key technical milestone for the company’s transdermal delivery platform.
  • Results support continued funding of ongoing comparative studies and guide next steps in formulation refinement and dose optimization.

Key Details

  • Study Design: Comparative mouse model evaluating a skin‑applied CPP (cell‑penetrating peptide) formulation of semaglutide against injectable semaglutide and untreated controls.
  • Interim Findings:
  • Animals receiving the CPP‑formulated topical semaglutide displayed a blunted glucose spike and faster return to baseline after an oral glucose challenge, similar to the injectable group.
  • Untreated control animals showed a pronounced blood‑glucose surge.
  • Blood‑glucose levels in the topical group remained stable throughout the observation period.
  • Technical Milestone: Demonstrates that CPP‑enabled transdermal delivery can achieve pharmacologically meaningful systemic exposure of a large peptide (semaglutide) in vivo.
  • Implications: Provides preliminary in‑vivo support for LIR’s platform to deliver GLP/GIP‑based therapies needle‑free, potentially expanding treatment options for obesity and metabolic disorders.
  • Next Steps:
  • Refine the topical formulation and narrow dose ranges.
  • Complete additional comparative studies already underway, including another GLP/GIP‑based therapy with results expected soon.
  • CEO Comment: “Even at this interim stage, we are encouraged by what the study is showing… it gives us a clear basis for the next phase of work, including refining the formulation, narrowing the dose range, and completing the additional comparative studies already underway.” – Edward Mills, CEO

Notable Quotes

  • Edward Mills, CEO: “Our CPP‑enabled topical formulation is producing a meaningful glucose‑lowering effect in a standard model. This is an important step because it supports the thesis of pursuing a needle‑free approach and gives us a clear basis for the next phase of work.”
Read the original news release →

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