What we do know is that UK and EU has formally accepted the new end points and that it’s a win in their books! If the US clinical trials registry is updated with new end points, will you agree that it’s a win with FDA as well?
You have a huge imagination you keep pretending the FDA has not bought into the amended SAP and endpoints, they have and thus can be determined if these endpoints have been met aka if approval is highly feasible.
What others have told you a million times here. The control arm crossed over on direction by the FDA because the treatment worked and its a lethal disease. One has to be an incredible dirtbag to keep patients in the control arm and have them die so Exwannabe on a message board can be satisfied. You would not let these patients die so you be more happy here now would you Ex?
So now that the FDA directed NWBO to treat the control that same FDA will not tell NWBO hey ooh dummy you blew the trial and treated the control arm at our direction ooh stupid! You should have let the control arm patients die so we can compare the old way. They did not say that Ex you know why? Because even the FDA has a heart. Capich?