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Lexaria's Human GLP-1 Study #5 Begins Dosing

1. Lexaria begins human study on oral DehydraTECH-liraglutide, comparing it to Saxenda. 2. Previous rodent studies show promising weight and blood sugar reductions with DehydraTECH-liraglutide.

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Why Bullish?

The initiation of human trials for a potentially innovative drug can positively impact LEXX's market perception. Successful results may enhance investor confidence and lead to increased stock value, as similar past studies in the biotech sector have seen stock prices rise significantly post-positive trial announcements.

How important is it?

The announcement of human trials is critical for LEXX as it implies progress in its drug development pipeline, which is vital for its valuation. The successful transition from animal studies to human trials marks a significant milestone, indicating LEXX's potential for future profitability.

Why Long Term?

The results from the human study will take time to analyze and report, likely impacting LEXX's stock in the longer term. Historical examples, such as the impact of successful clinical trial results on biotech stocks, typically show extended time frames for market adjustments.

Related Companies

Head-to-head human study comparing traditional injected liraglutide to first-ever oral DehydraTECH-liraglutide Study will investigate Pharmacokinetics and Safety KELOWNA, BC / ACCESS Newswire / April 2, 2025 / Lexaria Bioscience Corp. (NASDAQ:LEXX)(NASDAQ:LEXXW) (the "Company" or "Lexaria"), a global innovator in drug delivery platforms, is pleased to announce that dosing has begun as scheduled in its human study GLP-1-H25-5 (the "Study") that is comparing oral DehydraTECH-liraglutide to injected Saxenda®-branded liraglutide. On November 20, 2024, Lexaria reported on an earlier 12-week study in rodents which showed that with unlimited food available, oral DehydraTECH-liraglutide demonstrated a 5.88% weight reduction and an 11.54% blood sugar reduction as compared to baseline.

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