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powerwalker

01/15/20 11:06 PM

#230584 RE: TempePhil #230581

TP and Bio, thanks for your meaningful posts today.

Let's hope when the time comes for the FDA to rule on Biogen's Adu, it has enough info on 2-73 that it may perform a comparison of the two drugs as to which helps sufferers more and provides benefits to sufferers and the families thereof ... and it has enough courage to make that comparison public for all to see and examine.

This might be a little "out of the box" thinking for the FDA, but isn't that what it claims it is shooting for in its new wave of reviewing.


ANAVEX NOW ... MONO-STYLE ... RWEm for Life ... and for ALL AGES!!!

Biostockclub

01/15/20 11:27 PM

#230585 RE: TempePhil #230581

Thanks, Tempe,

Nice insightful thoughts. Let’s see if we get a fair shake from FDA. I think analysts are in our corner, more than in BIIB’s, and institutional investors coming along now too it appears, slowly. This could be a landmark case for the FDA going forward - continue scratching the backs of those within the system at the expense of patients and costly economic heavy burden or finally give it over to science and the underdogs if it can be proved that the science has more merit.

Lot of integrity and future outcomes riding on the backs of the men and women in approval power to uphold their jobs and our safety and economic prudence with honor and decency. Too much to ask in a civilized, democracy?

Time will tell.

Thank you for the analysis.
Biostock

nidan7500

01/16/20 9:08 AM

#230631 RE: TempePhil #230581

Good observation:

It seems like biib is trying to get around the system by pressuring/challenging fda to approve aaducanumab, and not prove the signal that they claim to see...by running a trial. Lol fda is being tested/trialed now! They are supposed to be the impartial judge/referee...we will see if they pass the trial! And not succumb to BP.



FDA are in a box of their own creation. Yet another repeated run at the Plaque variant solution. C'MON...IS THAT ALL YOU GOT???????. If they do not allow yet another BIIB trial w/very dubious history to run, thuS allowing-sponsoring BIIB sp RUN UP...(we really need a good look at where the $$$$ goes) or else they must come right out and say in public that this product is a loser...period.

The smartest thing they could do politically is do stringent PII testing get some REA DATA. BIIB are cleverly connected in the system and no doubt have their foot on the throat of the guy w/the money. There is no doubt in my mind they are all corrupted.

This is a true test of the FDA and the pay for play system. Timing is critical. IF TGA is going to be public w/ideas/plans for AVXL then this is the time to act. Such a move puts the FDA plan for BIIB in full view where conflicted interests are seen. One good thing about science, WHEN YOU GOT IT FLAUNT IT.