To those that know drug market better then I do
Assuming PAR passed phase 3 for iPps OA and a generic wanted to encroach, would they have to
a.) do trials just on OA patients with their own version of iPps - if so how long (time) from start to finish & how much $$
b.) do a trial to get their iPps version accepted by FDA then do all trials related to OA (like point a.) above (hence 2 different types of trials) - if so how long from start to finish & how much
it's all very complicated but you would assume PAR management would be all over this one would hope
Fiftyone Capital Update, page-23
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