is...still alive.
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Right you are, that's far more important use, ie. diabetes.
more important than even the pancreatic cancer focus.
Long ago there was mention of interest by Loreal (couldn't find anything recent); so, possible other legitimate reason for skin test (subcutaneous use)? not just as a skin patch.
Austrianova has ongoing collaborations with PharmaCyte Biotech Inc., a U.S. listed Biotech company (www.pharmacyte.com), with L’Oreal (www.loreal.com), and with a large number of other multinational companies.
Austrianova Secures Significant Investment from Real Tech Fund
Austrianova/SG Austria announced today that after extensive due diligence Real Tech Fund (Japan) has invested an undisclosed seven figure amount in Austrianova.
It was stated that all proposals passed and that an 8K detailing the meeting results would be available/filed in 4 business days.
PMCB SEC filings are available on the PMCB website.
https://ir.pharmacyte.com/all-sec-filings
SEC Filing Alert
10-Q: Quarterly report pursuant to Section 13 or 15(d)
OMG - FDA even requiring a new pig study!
Austrianova Thailand at BioAsiaPacific 2020
"Here's a snippet of our CPO's panel talk at BIO Asia Pacific 2020 on October 29th 2020"
Posted by Austrianova on Facebook 10/30/20, approx 5-6am
Video Interview and GMP Tour
Video is approx 7min38sec
Reference to PMCB IND & trial starts at 4min25sec approx.
No new revelation, except to acknowledge the possible trial start this year.
"On October 14, 2020, .... Amendment No. 3, Dr. Crabtree will no longer serve as Chief Operating Officer of the Company but instead will serve as Chief Scientific Officer of the Company...."
8-K dtd Oct 16
Invetech to develop GMP-compliant encapsulation by end 2022
TreeFrog Therapeutics and Invetech Expand Partnership to Transition High-throughput Stem Cell Encapsulation Technology to GMP System for Commercial-scale Cell Therapy Manufacturing
October 7, 2020 By Cade Hildreth
Christmas is coming, the geese are getting fat
Please put a penny in the old man's hat
If you haven't got a penny, a ha'penny will do
If you haven't got a ha'penny, then God bless you!
thank you, I missed that.
Anyone, what is status on FDA IND Fee?
For months there was sparring here re:
PMCB can't afford fee; there is no fee; Buyer of PMCB will pay fee; there is no fee; & on & on.
Do we know if there is a fee or no fee for our specific IND.
If there is a fee, is it due when IND is submitted or when approval is received?
If PMCB's IND requires a fee when submitted, then who paid it?
and Drug Master File has been accepted
FDA Formally Accepts PharmaCyte Biotech’s Drug Master File for Company’s Pancreatic Cancer Therapy
Question: is "30-Day" policy reset when answer to FDA request is provided?
or maybe Universities will develop their own testing
One university may have the best COVID testing operation in the U.S.—and tests students twice a week - BY LEE CLIFFORD (fortune.com) - August 29, 2020 5:00 AM CDT
...and 1 million in first seconds of trading
...but Cheers to the buyers of tens of millions shares
PharmaCyte Biotech Ready to Submit Investigational New Drug Application to FDA for Clinical Trial in Pancreatic Cancer
Click here to read the full article
Exactly! 40million shares are now in somebody's account.
5 million volume. Guess several people were ready.
That's the spirit Dewey!!
Austrianova announced their new website went live yesterday.
Getting ready for something? or just routine improvement?
Austrianova updated website
Look at those buys low .02s
Results of the 3-month Stability study were going to be positive or nothing would need to be written.
So even before we passed the 3-month checkpoint Facet knew what they were going to write.
All that PMCB should need to do is drop it off at the UPS dropbox.
Austrianova Singapore has just moved the laboratory
Austrianova Singapore has just moved the laboratory
Posted 8 hours ago on Facebook (as of 9:45am CDT, 06/16/2020)
This seems like good news to me, except the PR leaves it obscured.
Thank you, I also found and updated my 1st posting.
This means we should already have the data.
Instead of leaving doubt, why not just state in the PR that the data for the first 3-month test point is now available and can be included in the IND?
We should be past the first 3-month test point already.
A Walk Through our Manufacturing Facility
[posted on YouTube earlier today 5/23]
Austrianova GMP Facility
Nima Montazeri (reporting person) is not the direct owner, but can substantially benefit from and has significant influence over 95,262,015 shares.
The aggregate has reached the percentage threshold and must be reported.
[my layman's understanding/description / happy to be corrected]
nevermind, your board posting changed...
Wouldn't that indicate their IND was submitted Mar 14 or earlier?
Not everyone lives in USA under FDA control.
PrimeGen website - some things are finally happening.
Research continues to move forward, elsewhere.
Columbia Univ Rsrch - Kidney stone drug found to starve pancreatic cancer cells to death
I'm not a bio guy, but is there another possible use for CIAB?
I do wonder if Facet did the IND.
It was submitted.
FDA feedback (implying non-approval) was received.
and we are now looking at what needs to be done based on the feedback.
????
So the capsules and cells from the manufacturing run which have been tested and validated
and were to be from the same capsules/cells to be used in the trial
are now going to be boxed up and labeled
I have not lost my hard-earned money.
True it has not been available as soon as I wanted.
But it is not lost and as of today, circumstances indicate that I will be receiving many times more dollars than I ever hoped to earn if I had put my hard-earned money somewhere else.
Here's the IR Press Release link as distributed in their email this morning:
One lengthy part of the IND application preparation may result from the FDA statement: