A lot of bashing going on with the other board. I find it interesting that people are complaining about Leo and the number of PRs, SP etc. To me, it seems like a lot of work is going into applying to the FDA for the various designations, setting up the clinical sites and arranging for all of the agreements required to do so, coordinating the manufacture of the drugs for trials (B-OM, B, P and K) and then making sure they are meeting quality standards and at the same time putting out a lot of PRs, holding a shareholders meeting and fighting a law suit, not to mention pursuit of additional indications for B (gram neg) and whatever else we don't know about. That's a hell of a lot of work to handle all of those things, but I guess if I had my own money invested, I would be motivated to take all of that on as well.....I get the frustration with the SP, but these guys are moving things along substantially!
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