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Re: 236T568 post# 7290

Saturday, 11/22/2014 2:41:03 PM

Saturday, November 22, 2014 2:41:03 PM

Post# of 9895
Thank you for digging....which caused me to dig further.
It would seem that my former answer still stands because that is the way it was set up.

I will now try to explain as it was explained to me.

One may set up a cup program to mimic a trial....collect all the data.
Doctors wanted the CUP program......PVCT provided.
But what use is that data? It could not be used for any PII or PIII or for the FDA.
But you will be incurring the cost of a trial......millions......money they did not have when they started the CUP.
PVCT decided to set up the CUP to let the doctors treat the patients without the expense of running it as a trial. The decision was made to run it that way because of the risk, cost, and liability vs the benefit.
Since that is the way it is set up it, it becomes an expensive and time consuming effort to change the program to collect that data.....basically the cost of setting up a PIII. Back then they did not have the money to do that and because a CUP is more laxed an not as controlled the data becomes expensive PR use only. If you want trial data....run a trial.

Sometimes when I ask for info I get a minimum amount because they do not understand the context of what I am asking.


The above post is in reply to a post lifted off another board.
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