Thanks for sharing your thoughts Doc. Sorry for suggesting you were short AVXL - my mistake.
I appreciate your concerns about limitations of post-hoc analysis and why another trial is critical before approving a drug that will be used by millions. AVXL has learned a lot from earlier study and OLE data and should have no problem designing a new P3 that addresses shortcomings of previous trial. Also clear that it might not be successful. But, based on what we've learned to date, I think/hope it will prove Blarcamesine meaningfully slows cognitive decline and significantly improve the lives of both patients and their caregivers. I have not seen any AD drug with results as promising as Blarcamesine, but I'm sure there are some in development, which is why AVXL needs a sense of urgency and BP partner to get this across the finish line.
I still come down on the side of maintaining my investment and hope we get back on track over the next few months.