Lexaria Bioscience Corp. announced a new 2026 R&D program that includes a planned human clinical study, GLP-1-H26-7, evaluating SNAC-inclusive DehydraTECH-semaglutide tablet and capsule formulations versus commercially available Wegovy semaglutide tablets under fasted conditions. The 5-week parallel-group study is expected to assess safety, tolerability, and pharmacokinetics, with recruitment targeted as early as April 2026 pending ethics approval. Lexaria said results have not yet been presented and a final study report is expected in Q4 2026.
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