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Lexaria Bioscience Corp. - Warrant (NQ:LEXXW)

0.0400 -0.0200 (-33.33%)
Streaming Delayed Price Updated: 2:23 PM EST, Nov 20, 2025 Add to My Watchlist
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Press Releases about Lexaria Bioscience Corp. - Warrant

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Material Transfer Agreement Between Pharmaceutical Company and Lexaria is Extended
Via ACCESS Newswire
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Lexaria Bioscience Corp. Provides Strategic Update
Via ACCESS Newswire
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Lexaria Bioscience Corp. Announces Closing of $4.0 Million Registered Direct Offering Priced At-the-Market Under Nasdaq Rules
Via ACCESS Newswire
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Lexaria Bioscience Corp. Announces $4.0 Million Registered Direct Offering Priced At-the-Market Under Nasdaq Rules
Via ACCESS Newswire
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Lexaria Attending BIO International Convention
Via ACCESS Newswire
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The Global Revolution in Healthcare Driven by GLP-1 Drugs and the role of Lexaria Bioscience
Via ACCESS Newswire
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Lexaria's Technology Supports Higher Levels of the GLP-1 Drug Semaglutide in Brain
Via ACCESS Newswire
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Lexaria Attending the 27th Annual H.C. Wainwright Global Investment Conference
Via ACCESS Newswire
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Lexaria's Phase 1b GLP-1 Study Achieves Important "Last Patient Last Visit" Milestone
Via ACCESS Newswire
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GLP-1 "Arms Race" Broadens to Include Dozens of Companies
Via ACCESS Newswire
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Lexaria Provides Positive Interim Results on Partial 8-week Data from Phase 1b, GLP-1-H24-4 Study
Via ACCESS Newswire
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Ethics Board Approval Received for DehydraTECH-tirzepatide GLP-1 Study-Arm
Via ACCESS Newswire
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Lexaria's Strategic Business Pursuit of DehydraTECH-Liraglutide
Via ACCESS Newswire
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Lexaria Granted Two New DehydraTECH Patents for Treatment of Epilepsy
Via ACCESS Newswire
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Lexaria's DehydraTECH Technology Has the Potential to Unlock Accelerated Revenue Growth in the GLP-1-Industry
Via ACCESS Newswire
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Lexaria Reaches Patent Milestone - 50 Patents Now Granted Worldwide
Via ACCESS Newswire
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Lexaria's DehydraTECH-Liraglutide Human GLP-1 Clinical Study Supports Pathway to Potential FDA Registration as an Orally-Delivered Capsule
Via ACCESS Newswire
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Lexaria Provides Update on Material Transfer Agreement with Pharmaceutical Company
Via ACCESS Newswire
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Lexaria Announces Closing of $2 Million Registered Direct Offering of Common Stock
Via ACCESS Newswire
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Lexaria Biodistribution Study For DehydraTECH GLP-1 is Underway
Via ACCESS Newswire
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Lexaria Updates its Ongoing Human Study GLP-1-H24-4
Via ACCESS Newswire
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Lexaria’s Human GLP-1 Study #5 Receives Independent Review Board Approval
Via ACCESSWIRE
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Lexaria Announces $2 Million Registered Direct Offering of Common Stock
Via ACCESS Newswire
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Recent GLP-1-Industry Developments Highlight the Promise of Lexaria Bioscience’s Technology
Via ACCESS Newswire
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Lexaria Updates its Ongoing Human Study GLP-1-H24-4
Via ACCESS Newswire
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Lexaria's Human GLP-1 Study #5 Begins Dosing
Via ACCESS Newswire
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Lexaria's DehydraTECH-tirzepatide Oral Capsules Achieve Comparable Levels in Bloodstream as Eli Lilly’s Injectable Zepbound(R)
Via ACCESS Newswire
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Lexaria's Registered GLP-1 Study #4 Begins Dosing
Via ACCESSWIRE
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Lexaria Releases Annual Letter from the CEO
Via ACCESS Newswire
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Lexaria's Oral DehydraTECH-Tirzepatide Reduces Side Effects by Half with Comparable Efficacy Versus Eli Lilly's Injectable GLP-1/GIP Drug Zepbound(R)
Via ACCESSWIRE
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