Kbear....
"It just goes to show, poor results in the first instance doesn't necessarily determine the final outcome. Narrowing the focus to a smaller patient group resulted in accelerated approval being granted".
I find that comment interesting in that I have previously posted on the medical perspective of Prima's last results with 63 patients......I was told that because there was only 63 patients it's possible that the company
could be construed to have orchestrated the recruitment process for CVAC trials to give it the best chance of good results...Let it be said there is no suggestion that I think that is the case...
Anyway.......The median result of that trial is yet to be determined because simply, not enough people in the trial have succumbed to OC....
In light of a couple of recent approvals by FDA of OC research companies being given the go ahead to commercialise their products with quite a range of side effects has me, being an investor in Prima Biomed
somewhat bewildered.....
Given my limited knowledge of medical research protocol and procedure but being a graduate of the school of hard knocks, common sense tells me that CVAC is as good an option, if not better, than the last couple
of drug approvals.......
I am starting to sense that the FDA is starting to realise that OC treatment is a problem that it is not making any great inroads into.......
Just my opinion....Have a great break everyone....
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Kbear.... "It just goes to show, poor results in the first...
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