Lexaria Bioscience (LEXX) is pleased to recognize that the US Food and Drug Administration has approved Eli Lilly and Company’s (LLY) Foundayo glucagon-like peptide-1 agonist oral tablet for adult use in controlling obesity and weight-related medical conditions. “This latest approval from the FDA expands choices for Americans searching for the right weight control drug that best suits their needs,” said Richard Christopher, CEO. “Expanded choices within the historically limited oral weight-loss drug category increases opportunities for Lexaria to partner with the leading companies in the pharmaceutical industry to implement DehydraTECH technology to improve patient experiences including through the potential for reduced side effects.”
Meet Samuel – Your Personal Investing Prophet
- Start a conversation with TipRanks’ trusted, data-backed investment intelligence
- Ask Samuel about stocks, your portfolio, or the market and get instant, personalized insights in seconds
Published first on TheFly – the ultimate source for real-time, market-moving breaking financial news. Try Now>>
Read More on LEXX:
- Lexaria Launches New Human Trial to Advance Oral GLP-1 Drug Delivery Platform
- Lexaria Bioscience to begin new human clinical study in GLP-1
- Lexaria Bolsters Global Patent Portfolio With New GLP-1 and Cardiometabolic IP
- Lexaria receives five new patents, including two for diabetes treatment
- Lexaria Targets Booming GLP-1 Market With Enhanced Oral Drug Platform
