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My thoughts exactly. We can all speculate, but that’s the best we can do.
The only thing for certain is that this development continues to move forward.
Patience.
Go Team PharmaCyte!!!
lol RC...sorry to beat that dead horse one more time....but to improve or correct the problem(s), they’re “optimizing”.
Patience.
Go Team PharmaCyte!!!
That is a good point efood.
I wonder if it’s possible that such a cell demand,
as it would pertain to our development, could actually exists as an FDA requirement within their growth process parameters - unknown to us of course.
Whereas, in order to keep clinical material production efficacy, the cell populating MUST obtain a 100% supportive growth rate.
This would certainly provide constant supply for the production of clinical material.
Optimizing really is best.
Just my guess. :) :) :)
Patience.
Go Team PharmaCyte!!!
Good PR.
It was interesting to learn where the development is, and what it is exactly that they’re needing to accomplish. KW made it crystal clear what and why the implementations are necessary. It was also appealing to know the “strength” of our team that’s actively engaged in ensuring we will be submission ready.
- advances have been completed in the manufacturing process
- the encapsulation portion of the process is fault free and reproducible
- continuing runs in order to maximize the chances for a successful IND submission
- refining the steps to show a consistent reproducible and robust process
- refining the steps to ensure that the end-products of these manufacturing runs will convert the cancer prodrug ifosfamide into its cancer-killing form
- refining the steps to improve the growth of the cells obtained from the Master Cell Bank both before and after encapsulation takes place
- these implementation’s are in their final stages of optimizing their respective processes
- CT program progressing
KW and the rest of our team is absolutely committed to perfecting the work and processes necessary for an acceptable submission.
They continue to make PROGRESS that we should all appreciate. :) :) :)
Patience.
Go Team PharmaCyte!!!
I respectfully disagree.
I’m quite certain that along the way in the science and research of this development they identify and formulate to recognize the many variables and paths...as with most studies.
So, how the hell would they know what is required in advance?
I mean, do they have a crystal ball?
It’s a step by step process, is it not?
They cannot possibly know in advance who or what is needed until the time of each result within their studies.
Rather it’s Eli Lilly’s CEO, PharmaCyte, or some college freshman student, their assumptions and expectations throughout research and development won’t always support findings or results.
With assumptions and expectations you just cannot plan ahead.
Patience.
Go Team PharmaCyte!!!
An update on progress IS an update on “progress”. And as long as they announce that they’ve completed two to three more tasks on the list then I’ll be very satisfied.
I suppose we’ll hear a lot about Mr. Gillikin’s work and efforts.
Personally, I would like to at least hear that the cell testing has gotten past all possible points of contamination and are now safely contained.
I’m guessing most of the work documenting the required data (evidence gathering) coincides with every step of populating, freezing, and testing.
If that’s the case and all the final steps are complete, then in finalizing his work, Mr. Gillikin will probably have to explain of all that evidence as it pertains to each specific step.
Either way, I wouldn’t be surprised if the final compilation of ALL required documents takes a month or so to complete.
Would be nice if we hear that that is the bulk of work left to do and that we’re that close to submission. :) :) :)
Patience.
Go Team PharmaCyte!!!
Thanks for sharing that OldMusky :)
Yes,RC ...I’m hoping that that’s exactly what we’re going to learn.
A mentioning of Mr. Gillikin’s work in progress.
But Lord, more importantly, let it be news of the lab work and testing being satisfactory and completed. :) :) :)
Patience.
Go Team PharmaCyte!!!
I can see cGMP Validation easily adding 60 to 90 days.
Having joined us in December, we can only guess when they actually commenced working and collaborating with everyone....including the FDA.
I feel certain of one thing, and that there’s a ton of work and preparation to do.
Here’s KW again...
“...As I mentioned in an interview last summer, we’re almost there. Our checklist of items to be completed has been whittled down to just a few remaining items, and cGMP Validation provides us with the confidence moving forward to get across the finish line. It is imperative that our submission of the IND to the FDA is done flawlessly; therefore, cGMP Validation’s efforts will play a major role in ensuring that the IND we plan to submit to the FDA is as complete and accurate as possible.”
Patience. :) :) :)
Go Team PharmaCyte!!!
All in all, KW has been doing a good job.
For me, I've always held him accountable for one thing, and that's been to have put together a successful plan to get CiaB PC therapy to market...his job.
He doesn't keep the progress of our scientific developments moving forward. It's our entire team of scientists who are responsible for that.
Say what you want, but in fault-finding, using your frustration and impatience to justify blaming KW....well, you're only deceiving yourself.
Time and time again, its been said....this development is complex and time consuming. Is it harder to except than to understand? Perhaps, but hey, "you chose" this investment.
Reality is what it is... we truly are almost there when you look at how much time this project has been in development.
Hopefully, soon enough KW will have good news to share.
Patience.
Go Team PharmaCyte!!!
Poor Alex. Wished we were ready and able to help him.
God bless him and all the others.
Keep at it Team PharmaCyte!!!
Under development (as in R&D) one can “optimize” to improve a process.
Recent PR’s and email responses clearly imply Team PharmaCyte is continuing to make strides in their progress.
I, myself, have been loading more at .04 these past two weeks. :) :) :)
Patience.
Go Team PharmaCyte!!!
No, we’ve just got to get the FDA blessing for the IND.
...not putting the cart before the horse in my personal step by step expectations.
We’ve got no trials, NO NOTHING, without our IND blessing.
Patience.
Go Team PharmaCyte!!!
Amazing progress indeed!!!
But it’s obvious you’ve missed out on some of their announcements. Or maybe you’ve just forgotten what KW mentioned about where their focus has changed to.
Either way, you might wanna know that they are 100% focused on their PC therapy.
If successful, then you can be rest assured that attempts to resume the other developments will immediately follow.
Patience.
Go Team PharmaCyte!!!
And neither should anyone else....but my mentioning this goes without saying, I’m quite sure.
We all know better.
I look forward to hearing back from IR to confirm this information, as I’m sure everyone else will as well.
All in all, I do appreciate the post.
Go Team PharmaCyte!!!
You think?!!!
Where have I heard that before? :)
Go Team PharmaCyte!!!
Just don’t expect a bounce from it...the GMA “mentioning” is/was more significant than talking about something that’s not even acquired yet....just sayin :)
Can’t we just be engaged in the progress and not interrupt what’s unfolding? :) :) :)
Patience.
Go Team PharmaCyte!!!
“”.. An experienced biotech CEO would have had this to trials 2 years ago..””
No other CEO could have made a difference....come on, Bio. You know that.
It’s about the progression of knowledge in science, not the experience of a CEO.
So, would you then say... “any other group of scientists and doctors would have had it to trials 2 years ago”? ... I would like to think, no.
I believe we have “the best” team working on this development...this complex and time consuming development.
Let’s continue to allow them the time to make more great progress. That final round of progress needed to underpin “a successful submission” of that ever so allusive IND. :) :) :)
Patience.
Go Team PharmaCyte!!!
lol blah blah blah
Sheeeze!...so now we’re passing up the $11 target?!!!
imo it’s nothing more than a continuation from the hype pump machine. I pay no mind to those blaring bullhorns.
I just keep being patient and wait for material events...one at a time.
Slowly but surely we’re going to continue to climb. :)
Patience :) :) :)
Everyone have a great weekend!
Go Team PharmaCyte!!!
Yes Yes Yes ....totally in 100% agreement with you.
Getting past all possible points of contaminants is “key”. It’s my opinion that having positive test results is “the” true gate opener.
Positive test results. That’s it. :)
For me, that’s what changes the momentum in believing that PharmaCyte’s CiaB PC therapy “will be”.
Not IND submission (no brainer)...
Not setting up trials...(eezy peezy)
Not trial results (will work)....
Just positive test results is all I see we need that will put ALL we’ve been waiting for into motion.
Patience.
Go Team PharmaCyte!!!
Don’t let the volume fool you...there is no real volume.
It’s like esusun said before...it’s a fake market ...and until we get news it will continue to be a fake market.
3M shares is not even a half percent of total shares.
What you see is a steady continuation of crooked market makers and traders manipulating the price with their numbers game.
The real volume will come with real news.
Patience.
Go Team PharmaCyte!!!
The bride will come, but ONLY when she’s ready. :)
Patience.
Go Team PharmaCyte!!!
deal wasn’t done until after end of year
Bio is right...and equally the same, your first remark answers your question.
Patience.
Go Team PharmaCyte!!!
lol The pps will take care of itself.
Patience.
Go Team PharmaCyte!!!
lol And that’s what was said about the MCB....yet, here we are with that successful production behind us.
To some degree, this same kind of ranting has gone on for “all the progress” that’s been made...and it gets you nowhere.
Give it a rest!
We ARE at the end, and it’s IND or bust.
Patience.
Go Team PharmaCyte!!!
Patience :)
Go Team PharmaCyte!!!
LOL...that’s a good one Tulla
And yes, MAGA!!!
Patience.
Go Team PharmaCyte!!!
I gotta admit mixer, rcstock’s Ciab reply was hilarious.
“Ciab is not a man” LOL
How one unconfirmed posted email response can create so much unraveling is hilarious.
No sense in hashing over your unmet expectations...it’s like beating a dead horse. Doesn’t it ever get tiring?
Again, we all know this therapy development is complex and time consuming. So, until the entire process is completed and the IND is submitted, then we can only realize that the development is still in its R&D phase.
It’s not unusual or uncommon to be in our position because as with most R&D phases of science and medical developments, there are always CEO’s with miscalculating assumptions and frustrated investors.
For the time being, there is only one thing that we can be certain of. And whether it’s good news or bad, KW will eventually announce the outcome of “our attempt” to submit the IND.
Patience.
Go Team PharmaCyte!!!
lol PLEASE STOP MAKING ME DREAM!!!
You know I hate the “cart before the horse” assumption postings.
Go Team PharmaCyte!!!
What???
Did you read how long the populating took?, or how the freeze and thawing was a success showing 100% usable cells after testing?, or that the processing data was completed, gathered, and compiled per the FDA guidelines were ready for submission, along with all other trial materials?
...because I didn’t.
I mean is that what you’re referring to in your reply?
That’s your rebut?!!!
lmmfao!!!
Go Team PharmaCyte!!!
I’m ok with either, so long as the correction, including any work and/or data that can be reclaimed doesn’t take more than 60 to 90 more days.
However, no one here really can say just how long the final work, its necessary official compilation, and the process to submit for IND really takes.
Any innocent guess or raging rant would be nothing more than ongoing speculation.
Patience. :)
Go Team PharmaCyte!!!
Yes, the facts and progress are continually misconstrued.
Solid points clearly made 1234...excellent post.
Hopefully, positive results from the populating, freezing, and testing will be announced soon.
Go Team PharmaCyte!!!
I'd like to also say thanks, 1234.
It is a presumption. But, it is all we have. It is our hope and intuition.
Our hope and intuition that after all these years, our amazing team of scientists and doctors will come out in the end successful, and finally take us into the IND.
Welcome back. :)
Go Team PharmaCyte!!!
Okay then...but we’ll miss you...NOT!!! lol