The FDA's statement to HGEN says everything we need to know. In its letter, FDA stated that it was unable to conclude that the known and potential benefits of lenzilumab outweigh the known and potential risks of its use as a treatment for COVID-19. HGEN's treatment has known risks that the FDA doesn't like, unlike Leronlimab that has no SAEs.
My comments are just my opinions and should NOT be taken as investment advice.
Register for free to join our community of investors and share your ideas. You will also get access to streaming quotes, interactive charts, trades, portfolio, live options flow and more tools.