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Thanks Pete. Hope all is well...
Thanks, will sticky. Pete can you post in Intro?
PharmaCyte Biotech Releases Medical and Scientific Discussion from 2016 ASCO Annual Meeting
PharmaCyte Biotech, Inc. (OTCQB:PMCB), a clinical stage biotechnology company focused on developing targeted treatments for cancer and diabetes using its signature live-cell encapsulation technology, Cell-in-a-Box®, today announced the release of 5 video presentations that captured PharmaCyte’s medical and scientific discussion with oncologists interested in participating in PharmaCyte’s Phase 2b clinical trial in advanced, inoperable pancreatic cancer. The discussion session was by invitation only during the annual meeting of the American Society of Clinical Oncology (ASCO) in Chicago.
Portions of the session were videotaped, and the videos can be viewed at: www.PharmaCyte.com/Media
Commenting on the medical and scientific discussion, the company’s Chief Executive Officer, Kenneth L. Waggoner said, “On behalf of PharmaCyte, I would like to express our sincere appreciation to all who participated in this event, particularly those who traveled from Europe and Thailand to make presentations. Special thanks to those oncologists who sacrificed their time at the ASCO annual meeting to play such a major role. The discussion period led by Dr. Hidalgo was informative and stimulating. We believe it will prove to be of great value to PharmaCyte as we move forward with our preparations for the Phase 2b trial in patients with locally advanced pancreatic cancer.”
In addition to senior management from PharmaCyte, participants in the meeting included Dr. Walter H. Günzburg, PharmaCyte’s Chief Scientific Officer, Dr. Brian Salmons, a member of PharmaCyte’s Medical and Scientific Advisory Board, Dr. Matthias Löhr, from the Karolinska Institute in Stockholm, Sweden and the Chairman of PharmaCyte’s Medical and Scientific Advisory Board, and Dr. Manuel Hidalgo from the Beth Israel Deaconess Medical Center in Boston and a member of PharmaCyte’s Medical and Scientific Advisory Board. Joining PharmaCyte at the discussion were Dr. Stephen Gately and a team from Translational Drug Development (TD2), Dr. Ronald L. Korn from Imaging Endpoints, and, most importantly, a number of leading clinical oncologists from cancer institutions in the United States and Europe.
The meeting began with an introductory slide presentation by Mr. Waggoner. This was followed by presentations from Dr. Günzburg and Dr. Salmons that covered the development of the Cell-in-a-Box® technology and the properties of the capsules produced using PharmaCyte’s platform technology. Dr. Löhr, who served as the Principal Investigator for the previous 2 clinical trials using PharmaCyte’s pancreatic cancer therapy, presented the results of the previous Phase 1/2 and Phase 2 clinical trials. Dr. Hidalgo then covered the elements of the design of PharmaCyte’s upcoming Phase 2b clinical trial. Following these formal presentations, Dr. Hidalgo facilitated an hour-long discussion in which the invited oncologists discussed the proposed Phase 2b trial and ways to improve its design.
I agree saladan2. We have GMP and the backing of renowned medical professionals. Prices are so low, it makes accumulation easy for those who believe. But as you said, you have to be patient and willing to hold no matter what.
"Only buy something that you’d be perfectly happy to hold if the market shut down for 10 years."
-Warren Buffett
Love your enthusiasm... :)
Great to hear ferenc! GLTU
Oh yeah... :)
Nice...
I am willing to wait as well. I figured 5-10 years when I first purchased over 2 years ago. Seems we are right on track with a long term expectation.
“For the millions of people worldwide who suffer from a disease of epidemic proportions, our treatment could relieve them of the onerous daily requirements for insulin administration and dietary restrictions and offer a life free from the very serious and even life-threatening complications associated with diabetes,” said PharmaCyte CEO Kenneth L. Waggoner.
Nice article. Thanks
Well, plans for trials are still on... My bet is on them happening. In fact, I don't see TD2 backing out either. I believe CiaB is just that good. Only time will tell. But the fact that they just met with a lot of doctors who may be part of the trials speaks to me... "Hold, wait and see."
That's just me though. I am risking a little for a potential big pay off. It's a risk I am willing to take.
Good thing Austrianova is a major stakeholder in PMBC's success. There are certainly risks here, no doubt. I knew that when I purchased this stock. If we get to trials and are able to demonstrate what CiaB can do, I believe we are golden.
Right on track with all the milestones, however. Those are more important than dates, imo. The way I see it, they are extremely focused in spite of the challenges with which they are faced. They continue to press forward. I have a lot of respect for this company.
No worries, I know what it's like to get too busy to keep up with the goings on... :)
What is more important than meeting dates is realizing milestones, imo. After all, this is an R&D biotech on the OTC. Funding is challenging especially at this stock price. I am very impressed that management has gotten us this far.
I believe the technology is so promising that we have major support in the proper arenas. This support comes primarily from front-line doctors. Very minimal financial support thus far but as more milestones are realized, we will get there.
I don't let delays discourage me as long as I can see the company moving forward.
4Q2016 is the update from the Marcum webcast.
http://wsw.com/webcast/marcum4/pmcb
Always like to see you post. Great resource, thanks...
Never say never...
Very nice presentation. Ken did a great job. So, Dr Von Hoff did participate in the trial design himself. Love that this is clearly stated in a public forum.
I think it's a worthwhile investment... It must be since sooo many micro-caps are willing to pay the costs.
Looking forward to hearing the presentation.
I this you are misrepresenting here. This PR from 2015 clearly states the following...
"Chief Executive Officer Kenneth L. Waggoner and Chief Operating Officer Dr. Gerald W. Crabtree will attend the American Society of Clinical Oncology's (ASCO) 51st annual meeting to be held May 29 through June 2, 2015, at McCormick Place in Chicago."
Today's PR, on the other hand...
"Chief Executive Officer of PharmaCyte will be a featured presenter at the 5th Annual Marcum MicroCap Conference on Thursday, June 2, 2016, in New York City at the Grand Hyatt Hotel. The presentation is scheduled to begin at 9:30 a.m. EDT and will be available via a live webcast. To access the webcast go to http://wsw.com/webcast/marcum4/pmcb.
Tune in!
Where did you find info on all presenters having to pay a $5000 fee?
Many shareholders will be listening in, I am sure...
Thursday, June 2nd, 9:30 am EDT.
http://ih.advfn.com/p.php?pid=nmona&article=71612545&symbol=PMCB
http://wsw.com/webcast/marcum4/pmcb.
It was not our current management who has done nothing but move us forward and been above board on everything.
I am not concerned and I have my money invested here...
You and Bio are right, imo. KW has been so consistent and my only concern was GMP, now that's a non-issue so longs really can't be rattled.
Yes, I was able to find some of the info I was referring to but I think most of it is in filings as opposed to PRs. What I was able to find so far is the corrections he made to financials in 2015. He also brought Liquard on board after the errors were found. I thought PMCB had also changed auditors but have not found anything on that yet. I don't have time right now to go through filings but as I find info I will share.
The key point I was making is that we have a new CEO who is willing to admit to and correct any errors he has found and he did it soon after being on board. He was brought on board 4Q2014 and the below was communicated not long after he took over.
I see no reason to hold him to previous managements mistakes especially when he has demonstrated the level of integrity he has with managing PMCB.
http://yahoo.brand.edgar-online.com/displayfilinginfo.aspx?FilingID=11112535-308677-314277&type=sect&TabIndex=2&companyid=89889&ppu=%252fdefault.aspx%253fcik%253d1157075
Here is a link to explain the only reasons messages are deleted. FYI...
If it does not meet the conditions listed on the link for being deleted, it can stand...
http://ihwiki.advfn.com/index.php?title=Handbook#Deletion_of_Posts
Since Ken Waggoner came on board 4q 2014, things have taken a different course. In fact, he made sure to go back and clean up previous filings. Due diligence...
We are under new management... Folks should be aware...
I think Dr Von Hoff's bottom-line is patient care. That is why he contacted us. He saw our results and was interested. That is public knowledge.
Also, I don't believe they would have set target numbers for patients if they didn't think they'd have enough. Remember this trial is being conducted around the world and we are networked with many doctors who have a patient pool. And our CRO is TD2.
I am not the least bit concerned about conducting suitable trials. Everything has been going as planned so far....
I think Dr Von Hoff and TD2 have more knowledge about the availability of patients for this trial than anyone here. So, I will continue to trust that the doctors know what they are doing.
And where are you getting your information? And why would you refer to these patients as leftovers?
None of my DD says that they can't go head to head. I can see many reasons that they would choose not to go head to head. And a big reason is Dr Von Hoff. He is a CELG consultant. He is working with all involved to get this treatment to patients and we must not forget he contacted us...
I think those concerns are addressed with the current trial design.
"Major factors in the overall trial design are:
-The clinical trial will be international (United States, Europe and possibly Australia), multi-site, open-label and randomized.
-Study sites under consideration in the United States include the Mayo Clinic in Scottsdale, Arizona, the Beth Israel Deaconess Cancer Center and the Dana-Farber Cancer Institute both in Boston, Massachusetts, the Baylor Cancer Center in Dallas, Texas, the City of Hope Cancer Center in Los Angeles, California, and sites in Germany and Spain.
-The randomization ratio of patients between the two study groups will be 1:1 (an equal number of patients will be randomly assigned to the capecitabine + radiation group and the PharmaCyte pancreatic cancer therapy group).
-As many as 84 patients will be required to complete the study, although fewer may be required based upon the data developed during the trial.
-Only patients who have locally advanced, non-metastatic, inoperable cancers and whose tumors no longer respond after 4-6 months of treatment with either the nab-paclitaxel (Abraxane®) + gemcitabine or FOLFIRINOX regimens will be eligible for the study.
Unlike the earlier clinical trials using PharmaCyte’s pancreatic cancer therapy where patients received only two doses of ifosfamide, multiple cycles of ifosfamide will be given to those being treated with PharmaCyte’s pancreatic cancer therapy. This will continue until the patients’ tumors no longer respond to PharmaCyte’s therapy or until treatment-related toxicity accumulates to unacceptable levels."
http://pharmacyte.com/pharmacyte-biotech-finalizes-design-of-pancreatic-cancer-clinical-trial-and-identifies-trial-sites-under-consideration/
I am glad you are looking into that.
I never believed that someone tries to talk you out of an investment for your own good. Not unless you are asking for advice and good advice usually comes at a price...
That's why I do my own DD. Doesn't cost a thing but my time...
Awesome post Bio! Will sticky this one for sure...
I am enjoying our progress thus far getting us to trials. If the price does not respond to positive trial results, then I'd be concerned. But all signs point to success from my perspective. I do understand that we don't agree here at all. But my money is staying on CiaB technology.
This has been really a great ride and each milestone is so exciting. Fast tracking would be awesome. PC is usually diagnosed in late stages. Would be great to have this available to all PC patients ASAP...
Thanks Rudy for a great post..
Rudy, again you make very valid points...
The Holy Grail...
Not until a buyout or we see results from our P2b PC trial. IMO
Great link Otsy. So good to see you, old friend. Hope all is well...
He approved the PR before it was released.... Hmmm... I imagine KW dots his i's and crosses his t's in all he does with this technology. Smart guy.