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Re: georgesk post# 138978

Monday, 01/29/2018 3:33:52 PM

Monday, January 29, 2018 3:33:52 PM

Post# of 462742
Sold some this morning expecting a rehash, but I see subtleties:

The most common adverse event (AE): mild dizziness
§ When pa3ents were first dosed with highest dose
§ Was transient and reversible


I take that to mean that AE being a cause for reducing dose may not be the case.

Supported also by slides 17 to 21 pointing to the differences in therapeutic concentrations and/or their effect is suspected to be genetic.

Best case, analysis is being completed and trial start dependent on thorough understanding of inclusion/exclusion criteria. Still not a proponent of the waiting for FDA etc. theory.
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