Friday, December 01, 2017 9:28:48 AM
Take a moment to ponder the gravity of this particular point. Some have opined that the start of the trials will not be a stock moving event. Of course, these are expected. If they start before end of the year there may be some relief rally to the extent that delay was baked into the recent slide. However that is not the point!
The point is the unveiling of the Trial Designs together with the FDA agreed endpoints particularly the Alzheimer's P2/3 design and plan.
Now if the FDA agrees that there are intermediate endpoints that could be reached that would provide immediate and safe relief to Alzheimer's victims, such as relief from insomnia, agitation, mood and other symptomatic benefits short of the penultimate goal of preventing (or slowing) decline of cognition and other traditional and hard to reach endpoints what would the New FDA be mandated by the 21st Century Cures Act to do?
How would this speed the development of A2-73?
How might the Market react to this highly achievable intermediate approval scenario?
I know many of you have carried a heavy risk load for a long time. Hang in there the reward may come in the next three weeks.
Good Luck to all Honest Longs.
Truth as Beauty is its Own Reward!
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