Lexaria Bioscience Corp. (NASDAQ: LEXX) Kicks Off 2024 With FDA IND Submission For Its HYPER-H23-1 Phase 1B Human Clinical Trial

• Lexaria, a global innovator in drug delivery platforms, just announced the submission of its IND application with the FDA for its HYPER-H23-1 phase 1b hypertension clinical trial
• This study will seek to evaluate the safety and tolerability of Lexaria's patented DehydraTECH(TM) technology, specifically DehydraTECH-CBD, in hypertensive patients
• Lexaria expects to build on success of its previous studies, which showed positive results and DehydraTECH-CBD's potential to have broad therapeutic utility

Lexaria Bioscience (NASDAQ: LEXX) , a global innovator in drug delivery platforms, just announced the submission of its much-anticipated Investigational New Drug (“IND”) application with the U.S. Food and Drug Administration (“FDA”) for its HYPER-H23-1 phase 1b hypertension clinical trial. The submission follows a successful pre-IND meeting with the FDA, an integral step in the IND's development and filing ( ).

Titled“A Phase 1b Randomized, Double-Blind, Placebo-Controlled Study of the Safety, Pharmacokinetics, and Pharmacodynamics of DehydraTECH-CBD in Subjects with Stage 1 or Stage 2 Hypertension,” this study will seek to evaluate the safety and tolerability of Lexaria's patented DehydraTECH(TM) and specifically...

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