Sold some this morning expecting a rehash, but I see subtleties:
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.
Thanks. I'm curious to see the opinions on this board of the content. Anything interesting jump out to you? At a high level it all looked familiar to me so back to waiting and holding.
On a less relevant note, every time I see their presentations, I really want to hire a PowerPoint guru for them. I know it's minor, but there are some bad slide designs/graphics in there.