L & G, Dr. Dhody will discuss the very successf
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(Total Views: 876)
Posted On: 09/11/2020 8:17:33 AM
L & G,
What part of very successful FDA meeting you folks don't understand ???
What pat of upcoming HIV BLA submission you don't understand ???
Have been a long for many years ... it has not ben easy (was buying stock for many months wen the price was collapsing all the way to the 30's cents handle).
Few more days ??? Few more weeks ?? Months ??? . Who cares ??? I don't.
Once again, some of us are investors, some swing traders, some flippers, some shorts.
As the case might be, one either believes or not.
We will be having more details about the meetings. Dr. Dhody will tell us what they are doing to complete the BLA in FDA's format and re-submit. Hopefully soon.
NP will tell us that we are progressing in talks with the U.K.:
So, no need to speculate, as I se it, the presser was written in English, plain and simple English.
We are advancing and our day in court will come. No need to get anxious for 6 days ... or weeks, as the case might be, if one is an investor, that is.
Quote:
Dr. Dhody will discuss the very successful FDA meeting concerning CytoDyn’s upcoming HIV BLA submission
What part of very successful FDA meeting you folks don't understand ???
What pat of upcoming HIV BLA submission you don't understand ???
Have been a long for many years ... it has not ben easy (was buying stock for many months wen the price was collapsing all the way to the 30's cents handle).
Few more days ??? Few more weeks ?? Months ??? . Who cares ??? I don't.
Once again, some of us are investors, some swing traders, some flippers, some shorts.
As the case might be, one either believes or not.
We will be having more details about the meetings. Dr. Dhody will tell us what they are doing to complete the BLA in FDA's format and re-submit. Hopefully soon.
NP will tell us that we are progressing in talks with the U.K.:
Quote:
CytoDyn will also provide an update on the ongoing discussions with the FDA and the U.K. Medicines & Healthcare product Regulatory Agency (MHRA) for leronlimab as a treatment for COVID-19.
So, no need to speculate, as I se it, the presser was written in English, plain and simple English.
We are advancing and our day in court will come. No need to get anxious for 6 days ... or weeks, as the case might be, if one is an investor, that is.
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