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Posted On: 12/20/2018 9:22:09 AM
Post# of 72443
FDA issues new guidelines for surrogate endpoints in cancer trials, talks about how important it is for companies to meet with them to be sure clinical trials are designed in a way that will make it possible for FDA to accept their results.
https://www.fda.gov/NewsEvents/Newsroom/FDAIn...628853.htm
As applied to IPIX, this will help when the Kevetrin oral formulation trials start.
BUT -- RIGHT NOW -- does this shed a little light on how incredibly important IPIX's statement that the FDA was "collaborative" is? Green light from the FDA really means something important.
https://www.fda.gov/NewsEvents/Newsroom/FDAIn...628853.htm
As applied to IPIX, this will help when the Kevetrin oral formulation trials start.
BUT -- RIGHT NOW -- does this shed a little light on how incredibly important IPIX's statement that the FDA was "collaborative" is? Green light from the FDA really means something important.
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