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Not sure, but someone else here had the same problem with e-trade
anyway TD ameritrade you cant put a market order in has to be a limit order
did you do a market or limit order?
100% in 3 days not to bad
Not bad at all up 32%
This feels different like back up to .04 at least
I think the dump is done time to wipe and repeat the upward trend
A little bit of volume and we will be right back up to where we should be
Strongly Agree
Kaboom coming soon
Your kidding Right?
I finally learned, sell at least half around .05 to .06, it changed my opinion of KW somewhat.
IMO agree spot on, I picked up a few more, never thought I would get averaged down to .03, seems like a gift from KW, just like politics, you can look at it both ways.
I agree oldmusky, but there have been confusing PRS that they shortly afterword delivered on too, so, I dont believe it is on purpose, but also, I dont get why they do that.
I agree esusun, I have seen this before, history repeats oversold imo
They have been working on that for 50 years, CIB only 20 years
Wrong, they cant keep the cells alive inside the human body like CIB can.
I dont think he cares about the price, he only cares about the company and how this will get to IND
The product can now, safely be put into humans
20 years is not long, difference now, we have a product because of technology advances, that can be mass produced, frozen, to keep the cells alive for extended periods of time until ready to be used, and shipped all over the world, nobody else can do that
If you believe in the tech YES
I will remind you later, when the price is .05, like I said KW is good at what he does
anyway see you guys when the price is at .06, I can only take so much of this, I have to keep my sanity, good luck longs.
patience, my friend, patience, diamond in the rough, imo and in some great doctors opinions
LOL yes remember esusun
Imo it will be funded by someone else, just like all the other small companies that have great products, very typical.
cheap cheap cheap .029 we will be back up to .06, ts just a matter of when, like clock work.
Brian, good time to load cheap price never seems to ever drop below .03
I just asked IR, we will see if they answer.
I would think the stability test would be in progress, or completed, but who knows, I am usually wrong about what
I believe here most of the time.
Yes, I was a little disappointed at the time and I did respond back.
Below.
I came to conclusion that IND would be submitted somewhat quickly based on a couple PR’s
11/25 pr
“While the release testing is being conducted, we’re working to finalize the Protocol, the Investigator Brochure, the Pharmacy Manual and the Angiography Guidelines. We are also engaged in a selection process for a vendor to handle our clinical drug supply chain. All of these tasks should be complete by the time we receive the data from all of the release testing being conducted on the first and second manufacturing runs.
“After we receive all of the results from release testing, we will enter the data from those results into our Investigational New Drug application (IND) and then submit an entire package of information and supporting documents to the FDA for our planned Phase 2b clinical trial in LAPC.”
LAGUNA HILLS, CA January 22, 2019 (BUSINESS NEWSWIRE) – PharmaCyte Biotech, Inc. (OTCQB: PMCB), a biotechnology company focused on developing cellular therapies for cancer and diabetes using its signature live-cell encapsulation technology, Cell-in-a-Box®, announced today that both batches of the company’s manufactured clinical trial product have undergone and passed all 10 of the necessary “release tests” required by the U.S. Food and Drug Administration (FDA).
11/12 pr
PharmaCyte Biotech’s “Release Testing” Last Critical Event Before Submission of Investigational New Drug Application
PharmaCyte’s Chief Executive Officer, Kenneth L. Waggoner, said of completing the IND for submission to the FDA, “Most of the work needed for PharmaCyte to submit an IND to the FDA has been completed.”
Here is what I received from IR back February 11.
With the successful completion of the 10 “release tests,” the work directly related to the manufacturing process was complete. The pyrogenicity test was not one of those tests. The actual pyrogenicity test itself is not complex, nor is it time-consuming, but the preparations for the test are. Accordingly, at this time, the entire test is in progress.
The conclusion that you had that once the 10 release tests were complete, the IND would be immediately filed is incorrect because the IND consists of other items in addition to information on the manufacturing process. For example, on the medical side of things, very important major documents such as the clinical trial protocol and the Investigators’ Brochure, to name just two, are also a very major part of the IND.
So, as you can glean from the above, the IND for a late-phase clinical trial like PharmaCyte’s Phase 2b trial in LAPC is far more complex to prepare than would be an IND for a Phase 1 trial.
The time that it will take to complete all of the outstanding matters for inclusion in the IND is uncertain at this time and thus the time that it will take to submit the IND to the FDA is uncertain as well.
Investor Relations
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Looks like i will have time to load up more shares.
Adding bunch more if goes to O FOUR the magic number
Nobody knows the death percent cause no one knows how many people get the virus and then get better without anyone knowing so that don’t get figured into the percentage
Pistol you in this too
Agree, but I think they are working on funding and I hope they get it.
Agree .04 and I am loading the ship.