Monday, May 21, 2012 6:19:41 PM
That's a nice announcement today for the science. It's very early clinical work - Phase I safety study with some secondary efficacy targets. I think the success rate from this point to a commercial drug is generally about 5% (requiring years and $ millions).
But the approach seems sensible - I guess if it can be shown that Newell's IP safely enhances efficacy of exitsing drugs then there will be a reason for pharma companies to be interested in it, possibility of accelerated route to market.
Would be nice to see it in the hands of something with corporate credibility.
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