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More bullshit breadcrumbs. When will one lead to anything?
No ORR, no control, total cherry picked data. And LP said there was plenty of money (From Woodford) to run multiple trials on Direct. Where are they?
LP is too old to reboot Direct after shelving it. She will get rejected for L from MHRA, go back and forth for a year with her dog and pony show while diluting more and pumping more money into Advent, then sell it just like Cognate.
Nobody pays attention to what that dipshit posts. Like his buddy biowhatever , it’s a wall of text saying nothing.
Good luck on your cancer treatment. Been there done that but with a proven approved treatment.
Why not F—- the company for not moving this forward faster, for not using the CDMO shareholders paid for the make it, for lying about Direct moving forward after they ripped off $100 million from their only real investor, for apparently picking a piece of crap publisher with clinical trial experience, for running out of ink in their printer for the 150 million sheets of paper they apparently needed to print out like a 90 year old grandpa prints out all their emails, etc.
Correct. Legit companies submit NDA/BLA to the FDA, not the MHRa.
Now compare institutional ownership, outstanding shares, pipeline, etc.
It’s not a coordinated attack to call a piece of crap a piece of crap. You act like submission = approval. Not unless they have submitted data they haven’t released to the public.
And yet they've run a trial for 15 years and haven't proven it does more than the placebo.
It's an investment that you haven't made anything on in 15 years. Back to the basic concept of money for you! Once you pass the part about investments as things to MAKE MONEY I'll teach you about supply and demand, as in there's no demand for a penny stock with over a billion shares that has no product. That's why barely a million shares trade a day.
Keep shillin'.
And dendritic cells are just an expensive, passive placebo.
There are probably 100 qualified CROs who could have handled the P3 for DCVax but the company did not want someone competent because they wouldn't have been able to pass the buck on failure and the charade would have come to an end years ago when the good CRO submitted the crappy data.
Or NWBO contacted a legit CRO and they said "Why are you wasting your time with this trainwreck? You should've pulled the plug when you go the futility recommendation from the DSMB. We can't do anyting with this."
From the updates:
From the updates:
Nope. I was commenting on the link given by blabla which explicitly said they were trying to raise the money so he could start the treatment. Why don't you go back and read the link provided?
Control arms have patient level data. At least valid ones in the eyes of the FDA.
We know you are an idiot.
He is not “being treated with DCVax-L” but I know your reading comprehension is lacking.
More bread crumbs. Way to go flipper. Remember all the links to big pharma back in 2016 or 2017 when NWBO announced a tiny combo trial with free Keytruda and everyone said it was a partnership/buyout?
Same shit different year.
Merck has nothing and wants nothing to do with NWBO. They have 10x the oncologists on staff as the ones that have already panned the data and trial. Do you think they didn’t do the same IF they even bothers looking at the company?
Delusional idiots on a message board don’t change that.
They should PR that the majority of the money they have pilfered from the public has gone to build out Cognate and Advent for LP to sell for her personal gain.
Your answer to providing patient level data is to show campus layout of a legit company? Wow you are an idiot.
Median age being equal is irrelevant. They need patient level data for the control arm to compare apples to apples. They don't have it which is why the ECA is bullshit and why the FDA requires patient level data.
Ever notice the 3 people who NWBO always parades around as success stories were in their 40s when diagnosed?
Age groups have only been broken down as <>65. The way the DCVax trial screened out so many patients, I'll bet the 40-50 year old age group was greatly represented in the DCVax trial.
Why didn't they release the patient level data? Hmmm.
It's 3+ years after data lock. They don't want to submit anything because then the gig is up.
Dr Bot, regurgitating the same tired attack day after day after day.
What a shill.
Show me the patient breakdown and the control arm they are comparing to. The FDA has made it perfectly clear that the ECA needs patient level data and needs to be defined prior to running the whole trial.
A tweet from an idiot is not data.
I'll wait.
Call it The Grand Delusion.
Yes, everyone is afraid that the company will submit an application to a tiny market like the UK that will get rejected 2 1/2 years after it SHOULD have been submitted, and months after the company SAID it would have been submitted.
"Trying to move up" on <400K volume because there's no interest in buying at the ask.
Just make up a lie and pretend DI told you.
What's two billion OS, anyway! It's coming. Or she'll rename the company, change the ticker, and sneak an R/S in and nobody but this board will notice. Then she can repeat it all over again.
He's talking about DCVax orphan drug status which it has had since 2002 (making it irrelevant considering they haven't applied for crap in the US and it's almost 2024).
It doesn't have Fast Track designation. Other dendritic cell vaccines for GBM do, like DOC1021. It's early stage though and doesn't work either.
Did they PR how awesome their publisher was?
Nice cherrypicked data like every other shill. I remember when all the shills were saying "I didn't sell so I haven't lost anything". Same goes for now. You haven't made a penny either unless you sold. How much have you sold?
Of course you've been around since 2015 and didn't buy any when this was above $5. Why not expand your prices to when you were hyping the cheapies in 2015-16?
It was 2.15 when you added more Jan 11, 2016
Or this gem
Yes one of the many slimy ass things this company has done to pump up the stock price so their cronies can dump it. Where do you think the billion shares has come from? Day to day business expenses? For the $100 million the company stole from Woodford, they'd be able to get their fictitious publisher to actually get crap right and submit something without having to dilute the hell out of shareholders, don't you think?
Your "facts" had nothing to do with what I said. Zero ORR is a fact for Direct. Did you even read the Direct resluts? It's not foul language to call a moron a moron. Liau is a great surgeon whose treatment doesn't work as a standalone therapy. She proved that with the P3. She is among the many doctors who tried to develop a treatment that didn't work. Most treatments don't or we'd already have cures for most cancers. Why do you think they are doing combo trials now and not curing all these people with L? Because it doesn't work and is expensive and invasive.
$150K in the DC area is barely a living wage. Poor for a doctor, actually. I work there. He probably commuted an hour to DC on $150K.
He can't read.
For what, you idiot?
Keep up with the conversation you moron. When I mentioned ORR and one of your little clone buddies told you to type a stupid comment, I was talking about Direct, which is as worthless as L. The tumors did nothing. That's zero ORR.
No little charts you are being fed are doing anything to change that.
We are talking about Direct you idiot, which had zero ORR. It was a safety study with the primary endpoint of number of patients with AEs. I could have saved them money and told them their placebo was safe.
The secondary endpoint was number of patients with tumor response and no patients had any objective response rate which is how a response is measured.
Again you don't understand basic stuff the dumbest of morons would understand, and you certainly don't understand anything about this company or it's sham products.
There was no JAMA article on Direct because they shelved it because it didn't do anything.
DCVax gets an immune response like grapefruit juice gets an immune response.