Sunday, November 08, 2020 6:01:56 PM
You characterize the slowness of the FDA as being "bad news", adding that the Europeans "do tend to take forever and cannot be trusted anymore than the FDA can".
The UK has already fast-tracked DCVax-L (a couple of years ago) and I have no doubt that when the results of the trial show that DCVax-L works it will be speeded through to acceptance a.s.a.p. Were the FDA to be tardy, there will be severe public pressure placed upon it to follow suit with the UK/Europeans.
That is hardly bad news - bad news would be if the trial failed.
I do not recall the earlier posts to which you allude but with several hundred messages being posted each day on this board, that is not surprising.
The UK has already fast-tracked DCVax-L (a couple of years ago) and I have no doubt that when the results of the trial show that DCVax-L works it will be speeded through to acceptance a.s.a.p. Were the FDA to be tardy, there will be severe public pressure placed upon it to follow suit with the UK/Europeans.
That is hardly bad news - bad news would be if the trial failed.
I do not recall the earlier posts to which you allude but with several hundred messages being posted each day on this board, that is not surprising.
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