Thursday, November 07, 2013 11:38:12 PM
With respect to the population studies in the ANCHOR trial, the FDA also appears to have entered into an SPA with another company for their drug after the ACCORD and AIM-HIGH data were publicly presented suggesting that these study results were not viewed by the FDA as substantially new scientific information at that time. And we are not aware of any subsequent data which should have changed this perspective.
Is this really azn-epanova? Are they basically saying if you rescind ours then rescind theirs?
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