FDA
-
-
-
-
-
-
-
Lexaria achieves primary endpoint in Phase 1b GLP-1 study
-
-
-
-
-
-
-
Lexaria Bioscience Corp. Announces Closing of $4.0 Million Registered Direct Offering Priced At-the-Market Under Nasdaq Rules
-
-
-
-
-
-
-
Lexaria reports reduced side effects in GLP-1 drug trial
-
-
-
-
-
-
-
Lexaria's DehydraTECH-Liraglutide Human GLP-1 Clinical Study Supports Pathway to Potential FDA Registration as an Orally-Delivered Capsule
-
-
-
-
-
-
-
Lexaria's Human GLP-1 Study #5 Begins Dosing
-
-
-
-
-
-
-
Lexaria Granted Two New DehydraTECH Patents for Treatment of Epilepsy
-
-
-
-
-
-
-
Lexaria Bioscience's (LEXX) Oral DehydraTECH-Tirzepatide Reduces Side Effects by Half with Comparable Efficacy Versus Eli Lilly's Injectable GLP-1/GIP Drug Zepbound
-
330,698 total articles have been posted to this entity.
Click Here to Sign-Up for StreetInsider.com Premium to View All

