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Yes, he’s that diabolical, but better Santa than NWBO if Ex’s $.61 YE pps prediction is to be avoided. I don’t know about YE, but I suspect we will be at $10-15 before 1Q ends next year.
Ex, is AF planning a holiday hit piece?
Happy, “If you want to hear God speak, read your Bible. If you want to hear God speak audibly, read your Bible out loud.” — Justin Peters
Dr. Low, don’t forget Gary’s previous post noting that the DCVax-L journal article may be in SNO’s peer-reviewed journal called Neuro-Oncology Advances published by Oxford University Press.
The reason for my comment concerning Merck having influence with the FDA is from articles like this one from Science Magazine in 2018. Scroll down to the “Pick a Drug” Section and select Seroquel XR and Zyprexa Relprevv from the drop-down menu. https://www.science.org/content/article/hidden-conflicts-pharma-payments-fda-advisers-after-drug-approvals-spark-ethical
Yep, it’s clear that NWBO’s success is in Merck’s financial interest, and the latter holds sway with the FDA. Now we’re getting somewhere.
Well, I do agree the pps should be around $5 today, but I don’t agree whose fault it is that it isn’t. The only legitimate “complaint” as I see it would be a legal one against people like Ken Griffith at Citadel and Adam F. at STAT News. Linda Powers made a strategic mistake several years ago in underestimating the strength of those intent putting NWBio out of business out of greed and disregard for cancer patients, but her excellent business skills and intellect overcame those obstacles where many others would have failed. I have complete confidence in her ability to bring the DCVax platform to market in the very near future, to reward long investors, and to prolong and save the lives of cancer patients all over the world. May God bless NWBO, the physicians involved in the trial, Advent, and all the RAs in the coming weeks and months. It may take longer than we expect, but the pps will be a fair one eventually.
jammy32, in general, some people are unable to stop complaining. For example, even after the UK approves the MAA for DCVax-L, many will easily find something else to complain about. There will always be complainers among us. If you have this type of personality, then be careful not to set the bar too low for yourself.
A photo was posted on Twitter ($NWBO), and the slides have been requested…
jammy32, the arrow for the drop-down menu next to the list of Chairs may not be visible when using certain devices, but you should be able to search her name and access the information. I’m catching up on posts and see that you already found it.
Hang in there. It shouldn’t be another decade.
Splinters?
I’ll take poor word choice for $1000.
LOL, but I’m betting Viking didn’t make that up.
Some investors will be on their yachts incessantly whining about how long it took to get there.
Gary, I hope that’s the way LL and company planned it. I believe it would play out perfectly and would definitely get the job done. Regards, Vince
FeMike, I’ve been in this since 2013. In the past, when the company shared anything other than a completed milestone, they would get sued. So even after the JA quiet period is over, I’m content to wait for however long it takes until a RA, approves, a possible partnership/BO is announced, or some other significant event is completed. I don’t believe that they are tight-lipped because they don’t care about shareholders. No, quite the opposite. IMO it’s because they are looking out for all parties’ interests. But I don’t think your scenario will materialize anyway. I think we’ll have some good news prior to the ASM and any proxy vote for additional shares. My wife tells me an area for personal improvement is my lack of patience, but when it comes to NWBO, I’m very patient. Deep down I really think UK approval is imminent.
What about NWBO?
Bob, if that scenario plays out, why would anyone vote to deny the company needed working capital and thereby increase the risk of losing their investment rather than have their shares be diluted? Certainly the share price would go down further if more shares aren’t approved. Please help me understand the logic here. Is the intent to force LP to come up with alternative solution, and if so, what might that be? I understand why someone might be angry and frustrated, but I can’t wrap my mind around why they would make it more difficult for the company to succeed.
That pretty much sums it up.
I got back in at $1.20 several weeks ago.
Absent BO or P, I would agree.
I am an online ESL tutor for this Iranian-American materials engineer out in California. After I told him about NWBO, he did a deep dive. The other day he basically came to the same conclusion as you have. He said they must be waiting for something and thought shares would be at least $15-20 upon approval in the UK.
Institutional investors increased holdings by +13.62% last quarter, based on disclosures of 11 investors. https://www.msn.com/en-us/money/
Endpoints that have been met cannot be unmet because journal article authors can’t agree on the final draft.
The Dutch have a good sense of humor. As I was returning to my hotel room in Amsterdam to get something I’d forgotten the concierge commented, “Like my mother used to say, if you don’t use your brain, you have to use your legs.”
The numerous threads recently posted concerning approval timelines in the UK have been excellent. Thanks to all who contribute.
All sarcasm aside, I believe he’s referring to a financial report.
Perfect. Thank you, Onco.
crude, hopefully the following statement from their June 9, 2022 PR addresses your concern: We recently completed the acquisition of EPI Health. EPI Health equips us with a robust commercial infrastructure across sales, marketing, and communications, as well as fully dedicated market access and pharmacy relation teams. Following the acquisition, we employ approximately 100 staff, including sales personnel currently covering 42 territories, and we promote products for plaque psoriasis, rosacea, acne and dermatoses. We also have a pipeline of potential product candidates using our proprietary nitric oxide-based technology platform, NITRICIL™, to generate new treatments for multiple indications.
Good question. I see Hoff already covered it. GL.
Tote bag. It even sounds funny. But neither the tote bag scandal nor the generic name saga will likely survive script editing.
tryn2, someone posted that obtaining a generic name is a prerequisite for any drug that is to be marketed after regulatory approval, or something to that effect.
Senti won Best Generic Name with lydencel.
Then let’s make it Adamsindaholdencel.
In the Holdencel family, Biwaitdencel
Great minds…
Bob, if I had to communicate an estimate of an event that I thought would happen in approximately 18 months, I could see myself saying “in coming months”. I definitely wouldn’t say “in coming years”. If I were a CEO, I doubt that I would say “in about 18 months” in this context because there are so many things that could cause delays that are out of my control.
My guess is that if the committee of statisticians drafting the applications for the RAs have access to the unblinded data, then they would be able to include additional data analysis that hasn’t been presented so far at the conferences. Would a JA publication assist the DMC folks in writing the application and increase the likelihood of approval? I don’t know. Maybe so, but not so much as to affect the outcome.
That could be better for shareholders as long as it’s a happy ending. If IWD/Dr. Zivic’s notion is correct, then we may wake up one day to $10 pps after approval rather than $3 after the journal article is published. This is a much better scenario for longs who decide to take some profit in the near-term. If this is how it plays out, I hope LP has another loan with favorable terms lined up so that she can push the proxy vote for the increase in AS until after the first RA approval. The wait won’t be fun, but it’ll be worth it.