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The PR this morning really adds to my excitement about our short (and long) term future. This new relationship cements very clearly the two “fem phenoms” ( to borrow from Maverick) in a way that each clearly believes and supports our product and it’s development and approval. BEST INVESTMENT EVER!
Looking forward to next Tuesday then? Lol
Next step maybe Dr Ashkan??
Wow, great information! Thanks for sharing.
I bought in today. I did some due diligence and I like the company and it’s concepts. If I understand most everything is pre- clinical. Is there anything special that I’m missing? Other than the outside investment which made the stock pop the last few days?
My bet is they do but my time horizon is longer if they don’t make year’s end.
Thank you for your thoughtful reply. As I posted recently to Skitahoe, (and I accept anyone else’s point of view as we all have our own opinions of managements clarity to this point) I am just going to be thrilled and expect nothing more or less than a PR in the next 30-45 days citing an accepted MAA.
Good point on the submission aspect of it. I’d like to then amend my last post and say I would be ecstatic and would be satisfied with nothing more or less than a PR stating acceptance of an MAA.
Again, maybe that’s why the 30-45 days of built in vagueness? Maybe they submit next week and, even if they don’t get an acceptance in 2 weeks, they’re giving themselves some wiggle room on acceptance??
Are you saying that you don’t believe that they will PR after they submitted? I still have faith that they will.
I will be satisfied with a PR saying they submitted in the next month to 45 days. I’m not expecting more and not expecting anything less.
After it’s submitted and accepted, that’s really not in their hands anyway right?
Sometimes being a little vague might benefit management by keeping nefarious folks off guard. Like I said, if they do what they say in their PR in the timeframe stated, I will be very happy and will continue to give management the benefit of any doubt in the future.
The statement they made supported the stock price at the time it was made and if they had, say, waited a month to state “we are submitting to MHRA tomorrow” maybe we would not be in a better situation today?
People were calling management out for not providing information on a timeline and management obliged our request. As long as they do what they say in the timeframe provided, I think most here are more than satisfied by their decision to PR- even if they can’t for some reason send the application immediately.
Thank you for saying exactly what I’m thinking as I try to parse his words. I feel like I should go back for another degree…
I realize that Poly LCIC was used in the most recent trials but, I’m trying not to get too hung up on it being the only immuno- stimulant out there. If I remember correctly imiquimod (and possibly others can be used?)
So many of these biotechs are taking “far longer than expected”. I’ve been waiting on NWBO forever (and still believe I will eventually come out with at least a 10 bagger upon approval). I hope your Cormedix bears fruit soon but I’m quickly finding out that unless you have the metaphorical “cure for COVID”, nothing happens quickly in the world of biotech!
Just bought a little more to add to my small position as this is too tempting an opportunity.
My thought is that you’re correct but my fear is that waiting for FLASKWORKS approval may add a lot more time onto an already long wait?
Not sure if mentioned here before but this 10q from NWBO is dated 6/30/23. A whole month plus has gone by since. I bet it’s very possible we see application(s) submitted within the next 50 days.
Sorry, not sure what you’re asking. Actinium as a radioactive atom doesn’t exist naturally and is extremely rare. That being said, the company, Actinium pharmaceuticals, uses radioactive elements combined with human antibodies to fight blood cancers.
After my sale last year, I’ve determined that my time horizon for this stock is a lot longer and also depends on how much the price will increase after an FDA approval.
Congratulations on your treatment success! I also share your enthusiasm with ATNM but had substantially reduced my investment about a year ago. (Needed some cash). I still feel that what I have remaining will yield a solid return. Good luck with your continuing good health and your investments.
Correction MMA=MAA. Maybe I had the NWBO team doing some mixed martial arts on the hedge fund’s leadership??
Yes sir, thank you! Numbers like that reinforce my belief that my patience will be rewarded.
I firmly believe that, though not submitted yet, our future submission will be absolutely bulletproof- and that is why we are waiting. Our group has often spoke that LP has one chance to get this right. I believe that NWBO has hired the best and the brightest to develop the BLA and MMA to give the company the greatest opportunity for success. I’m confident that, with the stellar results of the phase 3 trial and the 300 other patient’s data, the properly submitted applications will gain us fast approval!
Good things always take time and, while like everyone else I’d like good news sooner, I’m still willing to patiently wait. You can’t provide 600 people with a treatment that isn’t safe and EFFECTIVE!
I’m just speculating myself, but considering the approximately 300 in the phase 3 trial + maybe 50 in the specials program since the trial ended + maybe 100 compassionate use cases + according to your estimates say 35 people treated with other cancers, we have approximately 485 people treated with DCVAX L?
Am I correct in my assessment that approximately 500 people have received treatment with DCVAX-L?
Well I was just wondering about TOTAL patients (gbm and all others. How many would you think?
In your opinion, just “L”?
If one were to hazard a guess, how many people over the past 20 years do you suppose have received DCVAX for any condition?
Dr Ashkan and Dr Liau are the most humble of ROCK STARS that neuroscience has to offer. I strive as a health care professional to achieve their level of care and expertise!
As a CVS retail pharmacist, I can assure you that we receive items stored at -50 fFahrenheit relatively often. I don’t see us on a retail level ever giving a DCVax injection however. Maybe arranged thru CVS Specialty and delivered to an oncologist’s office, but probably not thru retail.
Dr Murthy??
The answer is contained within the question. “Self” identifies “self” in normal tissue. You essentially can not sensitize your own dendritic cells to attack other normal cells and tissue in your own body. Dendritic cells are designed to recognize and properly detect and respond to non self which displays non-self antigens.
I got it in one- THANKS ALOT FLIPPER (seriously please don’t do that again)
And then I woke up! Lol
As much as I am a proponent of NWBO and the value of their services, I agree. We can’t keep setting ourselves up for a fall.
Not that I think that the 3 million has to do with any BP but- if you’ve ever watched the show “Shark Tank”- sometimes the money invested by the “shark” is less beneficial to the entrepreneur than the influence gained by the shark?
This post should be stickied. It has successfully embraced my sentiments regarding the lawsuit and our potential as a group of ordinarily supportive shareholders to inadvertently destroy the very positive story we have with DCVax. Thank you Biosectinvestor.
Thanks for sending the article as feedback. I hadn’t had the opportunity to do that yet!
https://www.medscape.org/viewarticle/988563
The above link to continuing education sponsored by Novacure lacked any mention of the only GBM TRIAL to show statistically significant results in 20 years…Hmmm
Do we have to wait for MAA approval before we find out how nice NICE is with reimbursement?