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Ethics Board Approval Received for DehydraTECH-tirzepatide GLP-1 Study-Arm

1. Lexaria receives HREC approval for 5th Phase 1b study arm in Australia. 2. Approval builds on prior arms, advancing its drug delivery research pipeline.

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Why Bullish?

The approval for the additional study arm is a positive clinical milestone, echoing past biotech advances where incremental trial successes boosted investor sentiment.

How important is it?

The news provides an incremental validation of Lexaria's drug delivery platform and progress in clinical trials, which could positively influence near-term sentiment, though it remains an early-stage development.

Why Short Term?

Clinical milestone announcements typically trigger near-term investor optimism, as seen with early-stage biotech companies progressing trials.

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5th study arm in 12-week Phase 1b Study receives lead clinical site approval KELOWNA, BC / ACCESS Newswire / February 24, 2025 / Lexaria Bioscience Corp. (NASDAQ:LEXX)(NASDAQ:LEXXW) (the "Company" or "Lexaria"), a global innovator in drug delivery platforms, announces it has received lead clinical site human research ethics committee ("HREC") approval that was required before dosing can begin in the 5th study arm of the Company's Phase 1b, 12-week chronic study GLP-1-H24-4, (the "Study") in Australia. This news complements similar news issued on November 13, 2024, when initial lead clinical site HREC approval was received for the first 4 arms of the Study.

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