Lexaria's DehydraTECH Technology Shows Significant Reduction in GLP-1 Medication Side Effects
TL;DR
Lexaria Bioscience Corp.'s DehydraTECH-semaglutide shows a 36.5% reduction in side effects compared to Rybelsus®, offering a competitive edge in GLP-1 treatments.
Lexaria's study demonstrates DehydraTECH-semaglutide's mechanism reduces gastrointestinal side effects by 43.5% and overall side effects by 36.5% versus Rybelsus® in an 8-week interim analysis.
DehydraTECH-semaglutide's reduced side effects could improve patient adherence to treatment, enhancing quality of life for millions managing diabetes and obesity.
Lexaria's innovative DehydraTECH technology not only cuts side effects significantly but also hints at a future where oral GLP-1 treatments surpass injectables in safety.
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Lexaria Bioscience Corp. has reported encouraging interim results from its phase 1b study, GLP-1-H24-4, showcasing the potential of DehydraTECH-semaglutide to reduce adverse effects significantly compared to the currently approved oral GLP-1 medication, Rybelsus®. The study, focusing on the safety and tolerability of DehydraTECH-GLP-1 formulations, found a 36.5% reduction in overall adverse events and a 43.5% decrease in gastrointestinal side effects with DehydraTECH-semaglutide versus Rybelsus®. These findings are particularly important given the widespread use of GLP-1 medications for conditions like type 2 diabetes and obesity, where side effects often lead to treatment discontinuation.
Richard Christopher, CEO of Lexaria, highlighted the significance of these findings, noting the superiority of DehydraTECH in minimizing unwanted side effects, which could lead to better patient compliance and treatment outcomes. The study's interim data also suggests that DehydraTECH-tirzepatide may offer a reduction in adverse events by as much as half compared to injectable tirzepatide, based on comparisons with historical data from injected tirzepatide trials. This represents a substantial improvement in patient experience and could potentially expand treatment accessibility for individuals who struggle with injection-based therapies or current oral formulations.
While the interim results are promising, Lexaria cautions that the full implications of these findings will only be clear upon completion of the study, with final results expected by the end of 2025. The company's DehydraTECH technology continues to demonstrate its potential to enhance drug delivery, offering hope for improved treatment protocols for patients requiring GLP-1 medications. The reduced side effect profile could have significant implications for long-term treatment adherence, particularly important for chronic conditions requiring sustained medication use. These developments in drug delivery technology represent an important advancement in making effective treatments more tolerable and accessible to patients worldwide.
Curated from NewMediaWire
