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Lexaria's DehydraTECH-tirzepatide Oral Capsules Achieve Comparable Levels in Bloodstream as Eli Lilly's Injectable Zepbound(R)

1. Lexaria reports successful Study #3 results for DehydraTECH-tirzepatide oral capsules. 2. Oral capsules showed better accumulation and 47% fewer adverse events than injections.

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Why Bullish?

The positive results indicate a significant potential market advantage, similar to how improved drug formulations often lead to higher stock valuations, as seen with other pharmaceutical innovations.

How important is it?

The announcement of positive PK results for a novel drug delivery system could significantly enhance Lexaria's market position and investor interest.

Why Long Term?

This innovation could lead to increased market share and sustained revenue growth for LEXX over time, reflecting long-term potential.

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More consistent accumulation demonstrated in bloodstream over a one-week duration with once-daily DehydraTECH-tirzepatide oral capsules as compared to once-weekly injection of Zepbound® As previously announced, oral DehydraTECH-tirzepatide also reduced adverse events by 47% compared to injected Zepbound® Lexaria's oral capsules worthy of expanded investigation as a viable alternative to injected tirzepatide. KELOWNA, BC / ACCESS Newswire / March 18, 2025 / Lexaria Bioscience Corp. (NASDAQ:LEXX)(NASDAQ:LEXXW) (the "Company" or "Lexaria"), a global innovator in drug delivery platforms, is pleased to announce positive pharmacokinetic ("PK") results from Human Study #3 or GLP-1-H24-3 (the "Study"), comparing an oral version of DehydraTECH-processed Zepbound® ("DehydraTECH-tirzepatide") to conventional injected Zepbound®.

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