Don't we already have enough shares shorted 22M+?; don't know how many today, I bet a million+ added today. Plus, those naked shorted shares ...only God knows how many are there. Anyway we will find out by the intensity of the squeeze shortly, imo.

I heard about the VW Mother of All Short Squeezes story before but I never knew how it was triggered with just under 12% shorted shares to cover with a mere 6% available shares to buy. I think the Company is playing the same strategy or even a more sophisticated one now. For example, a lot of my minions are shares are moved to Compushare! I think secureinvest or hoffman or hff a lot of us might be doing the sam or at least removed their margin platforms in their brokerage accounts. Way to Go NWBO!

Noted the words in capital letters. Agreed and theses are reflections of a lot of us as well. The Company is very UPBEAT for sure that everyone can see. Thanks for the timely input!

Cheapest shares on the earth when you look at its humongous potentials, imo.

I am the biggest of both of you, probably lost the most to the call writers; some to MRM I bet. But, sad MRM still is not happy as no one can be happy holding on to this stock; very unfortunate all doom to Du. Hi guys, I made my losses back with NWBO though. Who cares about losses. NWBO is still cheap now 75c if you want to grab some. ASCO is coming and their phase 3 readout is coming any day. Merck could buy this out to retain their Keytruda kingdom as the combo does wonders. TTE didn't believe in NWBO when I recommended last time; hope he changes his mind this time. It is a sure winner, imo.

We are putting buying pressure at 75c. We will constantly up it if needed. We are not using up all the dry powder though. Slow and steady.

My 2 rich minions are buying now.

ok we got it Judge! Glad Sojo concurred you!!

Off to the races!

I think LP loves to release news around middle of the week. What is today?

Mother of All Short Squeezes when erupts

No, I am not arguing with you. You are good. I did not speak with DI. I don't have a clue about the timelines for FW commercial cert.

Great, I am glad you agree the end goals are within their reach but (somewhat) not in their control. We are on the same page! But I am like Red; I just let the Company do their work.

FeMike/Boblob, do you agree that publication or MHRA cert or approval nothing is within the reach or control of NWBO? And if we all agree to that, peace will be here for all of us.

MMs take turns to walk it down while the volume is at its depth. They run out of playing the longs, lol.

And a number of my minions have accumulated shares more than the daily volumes these days. And they are rock solid in their conviction that DcVaxL is a success! Grand success, an earth shattering overwhelming one! Some are still adding more and more shares.

My minions are very good. They love to support the company whichever way possible. Their average is way lower than 70c. So, they are ok. Plus no one is nervous or scared of trial failure or that sort. The finish line is very very close, imo.

I am serious but you are joking it seems. I don't understand why you are sarcastic otherwise constantly. If you don't believe in, I will just get the hell out. Be serious!

I am constantly adding new minions into my group. They are buying 10k, 20k shares from the open market; thanks to the MMs for the cheap shares. I told these new minions they are lucky to get such a cheap entry when the rest of us endured a long journey.

Agency guidance documents even when finalized are simply guidance documents meaning they cannot be used in the court against the Agency by anyone if the Agency did or did not follow their own guidance some day at a later date. The same guidance cannot be used by a plaintiff demanding adherence by the Agency as well when finalized if the Agency chose not to follow some day. These guidance documents are guidance documents only, good to have to understand at times the mode of operandi, as long as things go good both sides. LL and LP commented to the draft guidance and LL might want to see thru her comments are addressed. However, Pazdur et al published their approach, in my opinion, in a more concrete way than what could be in the final guidance, kind of addressing both of their comments, as their new policy accepting External Controls openly recently in the Annals Of Oncology. They went on and on in that paper explaining all different scenarios what they would accept on how one can use ECs and apply seeking approvals. When I read their paper, I get a feeling that paper was written 100% keeping NWBO and DCVaxL in their heads. What more we want now in terms of finalizing that guidance document, imo? Agency choose sometimes not to finalize to overwhelming number of complex comments or take longer time when they are not ready to address some. I don't think NWBO expects any more confirmation from FDA any longer on the guidance other than the actual approval now executing their current policy, sticking to their approach of accepting ECs what they agreed to in that paper, I bet. It is their current policy now as the paper clearly explains. Agencies give more weightage to their on going policies than the guidance documents. Policies are developed only to fix the guidance documents some times. Of course MHRA approval might come along or ahead as they have openly updated the new endpoints in their clinical registries already or we might get all 4 RA approvals thru ORBIS or so. Irrespective of when the TLD or publication might come thru, I am for the RA approvals better than anything else because approval is the ultimate ticket for us to see the therapy reaching the patients anyway. Looks like we got a lot of PRs awaiting.

good inference, very possible, thanks Chiugray.

ok, I see, I got it better now! Thanks Bio!!

wow bio, great find! 150 days accelerated review interrelated with NICE simultaneously everything started just after 10/5/2020 dcvaxl data lock. Can all the rolling review be kept confidential? Is that what happening? Interesting if so.

while the FDA is ok with the External Controls, why don't we just ask them to grant us approval ahead of publishing trial results, lot of times that is the norm anyway. And I guess that is the path the Company has chosen now, which is really good for the Longs like me and my minions; because this way our investment is more secured away from the clutch of the short thugs, imo.

great, thank you as always!

wonderful piece of info, thanks RnH!

We are, with all we can now a days though we want more and more.

Power Hour is coming. It could do the trick.

Thanks VI. But glad the MMs and their clients are finally picking up cheap shares. Hope their other clients start covering before it is too late. But do the MMs care about them? Hell no, the MMs are there to make money in all different ways.

bids are coming in!

BMY terminated NKTR partnership; NKTR failed melanoma trial

https://finance.yahoo.com/quote/NKTR?p=NKTR&.tsrc=fin-srch

https://www.marketwatch.com/story/short-sellers-are-scarce-and-thats-some-of-the-best-news-the-stock-markets-had-lately-11646993331?mod=home-page

hyperopia, is the Validation Work = Compatibility Testing? Looks like Compatibility testing is done and applied for Flaskworks Certification, imo.

Viking, your guess is my guess too that there may be no abstract/late breaking no such presentation from us at ASCO because we might hear the TLD already prior to ASCO; but ASCO participation will be a big time exhibiting and may be the best buyout venue for us this time. How? Let me try. ASCO comes 6/3-6/7/22. The ASM must take place before June 18th to meet the 13mo timeline since the last ASM. They should give us a month notice to do proxy voting etc for the ASM and that should fall around May 15th. When it is a proxy voting, it means we should hear TLD good news on or before May 15th. It means we should see good news either Flaskworks Cert and/or Publication/MHRA approval that should come before May 15th. There is plenty of time to see either or both by 5/15, imo. And the Company has money thru June. The moment they release TLD, they can sell shares to Streetersville PIPs and raise more money at higher share prices. Looks like Publication/MHRA approval is the thing that we are waiting on and can come any day. DI said Flaskworks cert could come earliest by the month end or early next month. All in all interesting times ahead!

but the MMs specifically NITE determined to keep it either low or neutral the share price until the very last minute.

Dr. Bala, LG and Dr. Boynton are soo energetic for their age don't know where they get all the energy from; may be the overwhelming DcVaxL data that gives them all the youth fountain to see reaching the finish line and beyond. They work round the clock like a lot of associates they have I know who are really young and of course energetic as well.

we are having a feast today! Hope the MMs feel the pain soon for floating fake shares.

we thank both the Lindas; neither of them are wrong!!

One of my minions is adding today; he wants 200k shares; can scotty get him cheap shares?

Our goal now is to make the shorts starve for NWBO shares. And it is happening in front of our eyes. If you don't see it, just give a few more days, then you not only will see it but also will feel it.