Lexaria Bioscience Corp. (Nasdaq: LEXX), (the “Firm” or “Lexaria”), a worldwide innovator in drug supply platforms, is happy to announce the engagement of the contract analysis group (“CRO”) to execute and report on its 2026 animal Examine #1 (GLP-1-A26-1) that can consider various formulation enhancements utilizing each DehydraTECH-semaglutide (“DHT-sema”) glucagon-like peptide-1 (“GLP-1”) compositions and DehydraTECH-CBD (“DHT-CBD”) compositions to discover the potential for added improved efficiency in addition to stake new mental property (“IP”) claims (the “Examine”).
Contracts with the CRO have been signed, supplies sourcing is underway, and Examine design is being finalized with the purpose of starting dosing inside roughly 60 days.
“The worldwide arms race in diabetes management, weight reduction and different GLP-1-indicated areas of therapy is intensifying with latest new oral medicine being authorised by the Meals and Drug Administration (“FDA”),” mentioned Richard Christoper, CEO of Lexaria Bioscience. “With tens of billions of {dollars} in new annual income quickly anticipated within the sector, there has by no means been a greater time to stake new authorized IP claims with a view to provide the pharmaceutical business improved efficiency together with lowering unwanted effects, whereas enhancing Lexaria’s chances of changing into an indispensable supplier of improved drug supply expertise.”
Whereas ultimate design parameters of this Examine are ongoing, it’s anticipated to make the most of Sprague-Dawley rats with 8 to 11 separate arms evaluating various completely different novel compositions. Blood samples might be taken at a number of timepoints by means of an 8-24-hour post-dosing interval to quantify the pharmacokinetic efficiency of every composition. As well as, the Examine may also measure drug concentrations within the mind since DehydraTECH has, up to now, evidenced obvious superior absorption of energetic elements into mind tissue, an space of intense curiosity as a result of the truth that GLP-1 drug efficiency is more and more understood to incorporate and even rely on involvement of mind neurochemistry, thus making mind biodistribution important. There might be one reference arm utilizing an present DHT-sema composition and one other reference arm utilizing an present DHT-CBD composition. Lexaria intends to leverage the wealth of examine knowledge that we’ve got amassed from earlier work by using our proprietary historic knowledge and the reference arms as baseline comparators to the present Examine outcomes as we seek for areas of superiority.
One of many novel aims of this Examine might be to guage different/additive formulations to SNAC (salcaprozate sodium) which is at present in use by Novo Nordisk® with their oral Rybelsus® and Wegovy® pill merchandise. If Lexaria is ready to set up novel new formulations with superiority to SNAC, we could possibly register new patents and create priceless new proprietary IP and an business different to SNAC that may very well be of curiosity throughout the keenly aggressive GLP-1 sector.
Lexaria will replace its stakeholders as soon as dosing has begun. The Examine is absolutely funded from present company sources.
About Lexaria Bioscience Corp. & DehydraTECH
DehydraTECH™ is Lexaria’s patented drug supply formulation and processing platform expertise which improves the best way all kinds of medicine enter the bloodstream, at all times by means of oral supply. DehydraTECH has repeatedly evidenced the power to extend bio-absorption, cut back side-effects, and ship some medicine extra successfully throughout the blood mind barrier. Lexaria operates a licensed in-house analysis laboratory and holds a strong mental property portfolio with 65 patents granted and extra patents pending worldwide. For extra data, please go to www.lexariabioscience.com.
CAUTION REGARDING FORWARD-LOOKING STATEMENTS
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INVESTOR CONTACT:
George Jurcic – Head of Investor Relations
ir@lexariabioscience.com
Telephone: 250-765-6424, ext 202









