Replies to post #735290 on NorthWest Biotherapeutics Inc (NWBO)

[RobotDroid]

Excuses excuses. 'Backlog' is an old one. What happened to the Lp lie about being 'fast tracked'??? What happened to FDA submission???? What happened to "fall"?????? Inept mute nonmanagement can skirt around any required pr since they decided to not do another one. Not reporting bad news is their forte. LPowerless said she would not pr until things are completed, but it appears nothing will ever be completed in 2024 and beyond. Instead, grift more shares, add 1 million shares a day to the float, and hide with heads up asses answering to nobody, ESPECIALLY SHARE HOLDERS. The only vote they will ever get from me is 'Worlds Worst CEO'. I would also happily join any class action lawsuit.

[Investor082]

Balanced perspective. I agree UK approval is pretty much a done deal. However, it’s what comes next (significant non dilutive funding) that will determine the long term direction of the share price. Otherwise we give up whatever gains we get at UK approval.

My bet is that LP will disappoint again. So UK approval may be the best chance to get out before significant dilution takes over again for the next couple of years.

[learningcurve2020]

Without a NICE mention yours is half an argument. 

[iclight]

The MHRA waiting for information from an RFI that NWBO can not give or does not want to give is not a material event.

"Please proved the patient level data for your external control arm."

If NWBO does not respond they can continue to dump shares and pay for Advent while their useful idiots provide made up excuses to various social media and websites (like this one). The MHRA can do nothing at that point.

[antihama]

It is fair to criticize NWBO pumpers for only discovering the MHRA backlog of applications months after talking up the 150 day process as at best it shows sloppy Due Diligence with rose-colored glasses

Guilty! although I wouldn't consider it pumping if one really felt that way.

[Steady_T]

Am I the only one that thinks a 1.7 million page MAA might make it one of the slowest MAAs to make through the approval process?

How many other MAAs are that many pages? How many MAAs have over ten years of trials and data to be examined?

[Nemesis18]

As I nearly a year ago, this 'vaccine's' application derailed almost immediately upon submission to the Regulator.
Furthermore, that the NICE would never make it a prescriptive treatment in the UK.

There's only one winner here, and it ain't going to be any of you here!

So learn from your mistake...