ReRead my argument how the two are intertwined.
IF the trial to confirm has "demands" upon those participants
which outpace the cost Anavex would place on sales (not covered by Insurance, likely)
then filling the trial may be problematic as those wishing to pay to try the molecule
will reduce the patient pool. That scenario would also reduce your estimates of revenue
since the price would be minimal to create that situation.
On the other hand, IF Anavex reduces trial demands or chooses a price point for sales
that encourages cost/benefit participation by patients then sales obviously suffer.
In either case Revenue you cite as "missed opportunity" income favoring AA over standard approval
would be relatively insignificant.
While there is a difference in the eligible pool in USA AA approval over the Australian experience,
those that anticipated the same revenue stream or misread those eligible for sales
the result is likely the same.....unrealistic expectations of revenue.