What I got out of PR was that once translated into Chinese that IND would then be Fast-Tracked into Trial Phases which would then that those results would be enhanced and used in coordination with other Trial Results which then in turn gets put into FDA Submission......

Let the Trials/Phases begin in any way shape/form/Country......the time started HOPEFULLY OUR YESTERDAY (Time Change) and they have their IND FILED & Fast-Tracked and getting the First Person Jabbed.....

JMO with my CAUTIONARY NOTE REGARDING FORWARD-LOOKING STATEMENTS........