With the benefit of hindsight, you might be right .
There was no logical reason U 12 AGvHD should not have got the tick of approval for emergency use, until proven otherwise.
The next decision once MSB applies for a BLA will show FDA true Color’s (as @otherperspective post todays highlights ) .
It will show whether they pull the strings or unfortunately are at the end of the Stings, of big pharma.
Puppets or puppeteers !!
A case for why FDA needs MSB to succeed, page-2
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