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Biotech / Medical : ADVR and ONLY ADVR
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To: Bernie Bildman who wrote (10)9/22/2000 8:21:39 PM
From: DAN LITTLE  Read Replies (1) of 278
 
I think if we get the IND without fast track initially, that we will get fast track after the safety phase (phase I) at the very least. The FDA may look at this with a very skeptical eye in the beginning (I think they already are/have). If we can just get into phase I and show safety and efficacy (of which I have no doubt we will) we may just see Product R on the market next year (as Dr. Hirschman has stated).
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