Lexaria Bioscience CorpLexaria begins dosing in a human study of its oral DehydraTECH-semaglutide, a key product development milestone.
Lexaria Bioscience announced that dosing began on schedule on June 14th for Human Pilot Study #7, a five-week trial evaluating two oral DehydraTECH-semaglutide compositions against Novo Nordisk's Wegovy tablets. The study is investigating safety, tolerability, and pharmacokinetic properties across three arms, comparing SNAC-inclusive DHT-sema formulations in both tablet and capsule formats to the commercially available Wegovy tablets. For the first time, Lexaria is using an oral tablet DHT-sema composition designed to mimic certain physical properties of Novo's Rybelsus and Wegovy tablets, and both test articles incorporate SNAC in a multi-dose, multi-week human study. The five-week duration is intended to allow achievement of steady-state drug concentrations, and results are expected to be reviewed by the pharmaceutical industry for potential commercial relationships. The study is fully funded from existing corporate resources.
Lexaria Bioscience CorpLexaria begins dosing in a human study of its oral DehydraTECH-semaglutide, a key product development milestone.
Novo Nordisk A/SNovo Nordisk's Wegovy and Rybelsus are used as comparators in the study, but no direct impact on Novo is stated.