Lexaria Bioscience Updates on Animal Study Progress
Written by Emily J. Thompson, Senior Investment Analyst
Updated: Jun 23 2026
0mins
Lexaria Bioscience provides the following update on Animal Study #1 that is evaluating a number of formulation enhancements using both DehydraTECH-semaglutide glucagon-like peptide-1 compositions and DehydraTECH-CBD compositions to explore the potential for additional improved performance as well as stake new intellectual property claims. The Study is on schedule and dosing began on June 10, as planned. Barring any unforeseen interruptions, Study results are currently expected by early September. One of the novel objectives of this Study is to evaluate innovative alternative formulations to SNAC which is currently in use by Novo Nordisk with their oral Rybelsus and Wegovy tablet products. If Lexaria is able to scientifically evidence novel new formulations with similarity or superiority to SNAC performance enhancements, we may be able to establish valuable new proprietary IP and an industry alternative to SNAC that could be of value within the keenly competitive GLP-1 sector. To this end, Lexaria is pleased to report that we have already filed 3 new patent applications that anticipate our latest technological improvements in this area. The Study is utilizing Sprague-Dawley rats with 11 separate Study arms evaluating a number of different novel compositions. Blood samples are being taken at multiple timepoints through an 8-24 hour post-dosing period to quantify the pharmacokinetic performance of each composition. In addition, the Study will also measure drug concentrations in the brain since DehydraTECH has, in the past, evidenced apparent superior absorption of active ingredients into brain tissue, an area of intense interest due to the fact that GLP-1 drug performance is increasingly understood to include or even depend upon involvement of brain neurochemistry, thus making brain biodistribution vital. There will be one reference arm using an existing DHT-sema composition and another reference arm using an existing DHT-CBD composition. Lexaria will leverage the wealth of study data that we have amassed from previous work by utilizing, proprietary historical data and the reference arms as baseline comparators to the current Study results as we search for areas of improvement. The Study is fully funded from existing corporate resources. Lexaria is also reports that on June 11, the company received its first Australian patent grant in Family #21 - Pharmaceutical Compositions and Methods for Treating Hypertension.
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About LEXX
Lexaria Bioscience Corp. is a Canada-based biotechnology company. The Company's patented drug delivery formulation and processing platform technology improves the way a wide variety of drugs enter the bloodstream, always through oral delivery. DehydraTECH has also evidenced an ability to deliver some drugs effectively across the blood brain barrier. The Company’s segment includes Intellectual Property, B2B Production, and Research and Development. It is advancing several research and development (R&D) activities in both preclinical and clinical programs. Its focus is the investigation and the incorporation of its DehydraTECH drug delivery technology with glucagon-like peptide-1 (GLP-1) and glucose-dependent insulinotropic polypeptide (GIP) to enhance absorption and reduce adverse side effects. The Company operates a licensed in-house research laboratory and holds an intellectual property portfolio with around 48 patents granted and many patents pending worldwide.
About the author
Emily J. Thompson
Emily J. Thompson, a Chartered Financial Analyst (CFA) with 12 years in investment research, graduated with honors from the Wharton School. Specializing in industrial and technology stocks, she provides in-depth analysis for Intellectia’s earnings and market brief reports.
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