just remember that in the nasdaq you have to divide by 2 the real volume is 1/2 of that. why -- because the nasdaq counts the sales and the buys.
i always like to hear the naive talk. all high level individuals in public and private are politically oriented, it is generally how that got the job in the first place. so if you think that the senior fda managment isn't in tune to the house and senate -- wellll just keep shorting. also, if the were going to crl or reject it iw would have happend. again keep shorting dudette.
the professionals, the experts, sent a letter validating the effectiveness of the treatment and saying it should be approved. some professional showed up at the adcom and did the same thing. the optomotrist leading the fda charge along with the optomotrists and witch doctors on the panel think otherwise. how long does it take to reconcile the differing opinions.
the proof is very noticeable but visual -- kids that are alive but shouldn't be and kids running around that shouldn't be. denying the obvious is pretty stupid.
the ones on the board will sleep very well because their intrepretaion of the delay supports their delusion. however, as i said in an earlier post the smart shorts understand the meaning and are leaving.
well we all agree with the last half of your statement but af has multiple sources that provide info and he takes a pretty good stab at things. i always give him the benefit of the doubt but he is wrong sometimes but a lot fewer times than me -- a lot.
and the smart shorts know it so they are closing is that this will be approved. now i have been saying for many months that this will be a contingent approval not full approval. what they are working and arguing over are the contingencies. srpt needs to continue and finish the test schedule for the end of 2017. what that other contingencies developed should revolve around tracking and measuring all the kids that are put on etep and then measuring them against the statistical norm for the progression of the desease. that would be appropriate. once again the fda hosed the options crowd and the rest of us have to wait. thanks fda
to override the farkas bs. why didn't she decide. so i guess the kids have to die. glad i don't have a kid with dmd currently not on the treatment-- i would be a little angry (read a lot angry).
On something that will make their life easier and longer -- way to go fda -- way to go janet -- double way to go douche bag farkas.
I agree with you on a 180 degree pivot they need to investigate if she doesn't. You and farkas need an update on the fdaisa law and the fda needs to be taken apart.
there was 1.5 mill in premarket there are 22.6 million as of the 15th and more at end of yesterday. they did not cover. they will cover over the next couple of days because the fda gave them the warning and the time to close. thank you fda
The original padufa was feb 26 then they moved it to may 26 get the g-d appfoval out and worst of all we have to keep looking at all the basher/short bs on this board --evan though this means there will not be a rejection or a crl and they are letting the shorts cover and escape. Son of a bi ches.
that was an earlier tweet go look at the latest tweet or was it facebook or was it cnbc or wait maybe it was the street --- no it doesn't matter 100% giuarnteed -- a locked bet