Bourbon...agree with your assessment...these are not random events
He has planned the sequence PR/NEWS/conferences to build upon each other over time, IMO. I expect each session/process step will incrementally build the credibility and content of medical science and AVXL competence. As you say, why throw big $$$ at P3 if you are doing a crap shoot as has been the case for years? With more data, results and plans being published the investor risk is mitigated and confidence builds. Brilliant.
From Bourbon's post. "Of course there has been reasonable speculation that what this is really doing is confirming the first P2a, with the doses optimized. "
If Missling does indeed do this, doesn't it warrant Accelerated Approval?
Maybe one of the "considerable" number of filings Fadiran was talking about.