SEC Form 8-K filed by Lexaria Bioscience Corp.
UNITED STATES
SECURITIES AND EXCHANGE COMMISSION
Washington, D.C. 20549
FORM
CURRENT REPORT
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Item 1.0 Entry into a Material Definitive Agreement
Lexaria Bioscience Corp. via its wholly owned subsidiary, Lexaria (AU) Pty Ltd (“Lexaria AU”) has finalized the terms of its Project Agreement (the “PA”) with Novotech (Australia) Pty Limited (“Novotech”) and the associated project budget for the purposes of Novotech acting as Lexaria AU’s clinical research organization (“CRO”) for its Australian clinical study “DehydraTECH Cannabidiol alone and in combination with glucagon-like peptide 1 agonists in pre- and Type II Diabetes” (“GLP-1-H24-4”). The effective date of the PA is December 2, 2024. Pursuant to the terms and conditions of the Master Services Agreement (the “MSA”) and the associated PA, Lexaria AU has the ability to terminate the PA with or without cause upon 90 days’ notice. The aggregate costs associated with the PA is ~AUD$5.1 million with certain initial start-up work associated with the PA having been completed under a Start-Up Agreement (the “SUA”).
Upon signing the PA, Lexaria (AU) is responsible for:
| · | Payment of 15% of direct costs associated with GLP-1-H24-4 (approximately AUD$414,600); and |
| · | Payment of 15% of the total pass through costs associated with GLP-1-H24-4 (approximately AUD$347,800); |
With such amounts being reduced by the fees that Lexaria AU paid to Novotech for the services provided under the SUA.
The description of the PA with Novotech is qualified in its entirety by the agreement that will be filed as an exhibit to the Company’s quarterly 10-Q Periodic Report.
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SIGNATURES
Pursuant to the requirements of the Securities Exchange Act of 1934, the registrant has duly caused this report to be signed on its behalf by the undersigned hereunto duly authorized.
LEXARIA BIOSCIENCE CORP. |
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/s/ Richard Christopher |
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Richard Christopher |
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CEO, Principal Executive Officer |
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Date: December 18, 2024 |
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