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Den - I am guessing you missed the gist of my post. What I believe is that if a buyer group offered the vast majority of the outstanding shares 1 to 2 dollars they would take it. This would essentially be a hostile take over with very little the company could do based on current cash on hand. I am not saying it is what would be best for the company but sadly believe this could be purchased at a very deep discount because most investors do not have your depth of understanding regarding the true long term potential before us. In essence we agree on the long term - I am simply pointing out a possible outcome here.
For me the million dollar question and literally the million dollar question is buy out. I mean a leading cancer company could put 1 or 2 dollars on the table and purchase the entire technology for under 500 million which would be a bargain. Not to mention Dr. K could make residual money for a very long time off his patents. If I were in the industry given the cutting edge technology in question that would be my primary pursuit. Now you might say Dr. K might not want to see for 400 to 600 million dollars - that s why they call it a hostile take over. That is the path I am chasing down with my spare time...... either way great for the shareholders. People way smarter than most of us are following RDGL and their end game is in the billions........ of that I am confident.
This is what happens when someone with weak hands and short term objectives dumps their position. What we are now seeing is smart people buying up their discounted shares. My guess is that we close ABOVE 20 cents today ....... let see if I am right. Because let s not forget, the technology works, the delivery process is sound and all that is happening now is the pieces on the chess board being put into the proper sequence. I am not worried at all and am CONFIDENT the true upward momentum has not yet occurred and sooner rather than later will happen. If you have the financial ability just sit back and relax. If your nerves are on end and you do not have the capacity to relax and what a show unfold - do what you must. I wish you all well and hope you make the choices for yourselves.
I am sitting with 3.8M shares and holding since ADMD ...... my goal is .6723 before IDE submission. This is a very exciting stock / company to be a part of. It is / was fun to flip for some but those who were able to see the true value of the technology understood the risk and now will if they are patient enjoy the reward. My hope is IDE submission is the very last day of June to keep the momentum going. We also need new fresh eyes, enthusiastic investors who like us see the reward potential. Keep in mind doubling your money or even a 50% return is an amazing year for any true investor portfolio. Stay strong, be patient understanding that this is part science, part art and part advertising at this point to educate and reward new investors
Why and where do you see the PPS between now and IDE submission? I have a few thoughts but would like to see if there is a consensus. We hit 31 / 32 cents back in 21. Do we meet, exceed or stay in that range this time around?
Still here as well - just watching and waiting for the series of pops. This is as real as it gets with these types of stocks. I have been here since 2014 and have enjoyed the progression over the years and sooooo happy to be here for their giant leap. Nice to see you are still here Catfigh and Hunter......
Email ---- @se for sweeden.......
+46 sweedish country code ......
The 911 is just people doing that to make others guess and talk etc. Just noise nothing more!
Dr. K and his team along with Mayo Clinic resources have dedicated their lives - their lives - not like us here like hungry birds waiting for profits to be deposited in our accounts - to creating and developing a product that can help humans and animals. I would be inclined to cut them some slack and if anything offer them moral support and encouragment. We take past set backs as a financial loss - maybe we have to explain our decisions to family etc. - but for them the set backs were much more personal and deeply felt - yet they yes again they got back up the next day and showed up for work - while we pointed fingers and wallowed in our financial losses. I wish there were a few more cheerleaders basic acknowledgment and greatfullness that Dr. K and his team and Mayo did not quite or give up the way some of you have! 4.8m shares and still holding no matter what happens if nothing more than out of respect for the RDGL team who are doing something I nor most of any of us on this board can set out to accomplish.
So why are people talking reverse split and or dilution? I am curious what has the rumour mill going......
AND it s obvious he is not good at math because he mistook -2.17% as 30%.... so honestly just ignore the guy.... he s probaly texting while walking from guatemala....
He is not trying to shake anything or buy anything.... he is not an oportunistic buyer / investor.... he is just someone with time on their hands most likely sitting there without much funds trying to vent his frustrations of life on RDGL. When people like that post just think of it as NOISE..... IF A TREE FALLS IN THE WOODS AND NO ONE IS THERE TO HEAR IT DOES IT MAKE NOISE? DO NOT BE HIS SET OF EARS.... JUST THINK OF HIM AS LONELY TREE THAT FELL AND SOON WILL BE MULCH
Chereb - Now I will agree with you there and share some of your concerns. Since we do not know exactly the conversation that took place it is hard to guess. For all we know MAYO was asked to support part of the submission with data and content and that is exactly what they did. I does suggest to me they either felt they had strong grounds to pursue this route and that they were somewhat surprised by the FDA decision. Either way the key here is that they did provide support and are on the team to get this over the finish line. I believe they will be great partners for the human trials piece when we get there to help shorten the process and bring all of their internal processes, best practices and accredidation to the collected data. Once they put their stamp of approval on the data for FDA submission it should go along way.
No but the MAYO CLINIC would not attach their name and reputation to a scam or fraudulent company. They have done their due diligence and come to the conclusion that RDGL might just might have a better mouse trap and they are willing to put dollars and cents with staff and reseach support behind Dr. K. You are all missing the point - this is not a sure thing but its sometihng a lot of smart people think is worth their time and life commitment to see all the way until the end. Take all of the emotion out of this and you have a technology - a managment team - and partners Mayo Clinic and others who have stood by Dr. K and still stand there today.... as will I.
I would let those in the KNOW handle it. The last thing the FDA needs is people asking them questions regarding a denial or positive outcome. Sit back relax follow the company news invest if you think its appropriate and be patient. If you really want to help the company offer to volunteer your free time to help out around the office.... take out the trash.... hand out flyers to vet clinics etc. That will have more of an impact than reaching out to FDA. We are investors not gamblers..... diamonds take time to grow even the ones made in labs these days take time.
Champana is NOT BEARISH he is emotional and there is a difference! The company did not overnight change or lose their subject matter expertise they simply were informed they did not check a box on an FDA form is all. The technology is the same - MAYO clinic did not abaondon them so why should we.... I mean you all? You are introducing emotion into a business transaction and YOU WILL LOSE every time you do so. Man up, look adversity in the eye and HOLD! Learn who you are as men.... do you have the courage of your convictions
What amazes me is that people actually have the time to follow invest and comment on companies they do not believe in... Honestly it just deminishes the impact of your comments to take the time to trash a BAD or IDIOTIC or MISINFORMED investment decision YOU made. This actually comes down to a lack of confidence in your decision making process not Dr. K. If you believe your decision making abilities and due your due diligence pushing aside the noise and focusing on what is actionable information.... this bump in the road is just that.... a delay in the inevitable result approval or denial of the product. We have not reached the point of taping out... we as a group of investors and corporate leadership are still in the fight. BOOHOO on all of you that did not make the profit you wanted TODAY and that you may have to wait. Its not like you are working or doing anything to contribute to their success other than passively invest a few dollars here and there on the hope someone elses work will make you money. SHAME on you for your lack of self confidence.
Champana - Harsh don t you think putting out his contact info..... I agree this was poorly executed but none the less. You either believe they have a plan or you dont.... you either believe their plan has contingentcies built in for situations like this or you dont. He is a focused leader on getting a product to market in a sea of RED TAPE.... We do not need a new face with possibly new ideas.... we need solid execution of a plan the right plan which I believe Dr. K has in mind. If you honestly felt this way you should call him yourself - then brief us all on the call and what was said and or not said. You sound emotional and as if betrayed.... This is business and a harsh one to say the least. Have confidence in the product the team and most of all their day in day out courage and perseverance. Hang in there it will be ok..... just my 2 cents and pardon the typos I am on a conference call for work and multi tasking
What the Tweet on Friday meant was just because you cannot see right now with your eyes a clear path forward....i.e. we did not get FDA approval it does not mean there is not a path to success.... which to me means they are not giving up just adjusting the route they take to ultimate FDA approval.
Not surprised - disapointed yes - but not selling.... just my 2 cents
Nope this is fake and you know it is.....
what we saw was MM dumping 5 million shares at .27 to .28 and then buying them back all the way down to .20 to sell to the flippers again. You just have to have faith in your plan and execute accordingly
This is just weak hands I would think
Today we close .27 to .2725 ..... with news being received from FDA on Tuesday and press release Wed or Thur imo.
My thoughts is FDA provides their response on Tuesday of next week with the 16th being tomorrow and Monday a holiday. Should be a very interesting weekend of anticipation. This only means you have to buy in today to have a chance of sharing in potential positive news next week.
Here what I am now showing so maybe a pre market trade for 1.6 mil?
Price
$0.274
Day's Change
0.0148 (5.69%)
Bid
0.274
Ask
0.2813
B/A Size
84009x3135
Day's High
0.2895
Day's Low
0.27
Volume(Heavy Day)
5,307,565
January 15, 2021 10:41am ET
What volume are you all showing? On TD it changes between 3m and 4.7
Price
$0.2825
Day's Change
0.0233 (8.97%)
Bid
0.28
Ask
0.2848
B/A Size
13542x50775
Day's High
0.2895
Day's Low
0.27
Volume(Heavy Day)
4,847,909
I already am LOL. The key here is to not buy and be emotional about the stock. This is a great company, they have a great product / technology but more imporantly a STRONG managment team commited to succeding. That is a great combination and worth our support and worthy of our confidence. Let this play out and have faith in the team. Mayo did their due dilligence and decided to invest time effort and soft dollars into RDGL. That is good enough for me to sit tight and let the FDA complete their process and providing our team with another stepping stone towards healing people one day with the cutting edge approach.
3,672,512 shares and holding!
So that means either Friday the 15th or Tuesday the 19th for their response based on weekend and Monday being a Federal holiday.
My take on the tweet is that FDA is doting the Is and crossing their Ts in anticipation of approval. No crystal ball but I would think the FDA response would be more detailed if they had any real issues regarding approval. Just my take ......
I agree but he and I have history going back to ADMD so I should be good. Trust but verify lol
champana - can you reach out to me directly 410 991 9804
what is the total outstanding shares for GLSI? Just trying to look at that amazing increase versus what we might be able to acheive based on our number of total shares.
Vivos Inc Completes Surrogate Lymph Node Testing Using Mouse Spleen Injections Demonstrating Uniform Perfusion and Stability
Vivos Inc.
Wed, December 9, 2020, 9:30 AM EST
Richland WA, Dec. 09, 2020 (GLOBE NEWSWIRE) -- Vivos Inc. (OTCQB: RDGL), Vivos Inc is pleased to announce today that it worked with Mayo Clinic doctors to design and then conduct tests on the injection of hydrogel into spleens in mice. This conservative animal model was designed to gain practical experience on our new indication for use of treating cancerous lymph nodes. The objective was to build on our previous animal injection procedures and to validate the confinement of the gel in the nodes.
These important results confirm that the injected hydrogel perfused uniformly within the spleen without leakage, which is a critical safety characteristic for RadioGel™. These tests complement our previous testing on rabbits at Battelle National Laboratory, on feline sarcoma at Washington State University, and canine soft tissue sarcoma at the University of Missouri.
Dr. Mike Korenko stated “We are gaining a wide breath of experience with laboratory and animal validation models to build a strong clinical foundation, which we believe will help us to gain the confidence of the FDA and the Mayo Clinic administration to agree on a plan for future clinical trials.” We remain focused on securing the Investigational Device Exemption (“IDE”) from the FDA and believe that this can be achieved on or around the end of the 2nd quarter of 2021.
Someone is blocking the ask for a reason - to keep shares priced low. There in my mind is no other reason for a such a large block on the ask side. If you remember that same block was there last time as well. My thought is they do not want this to fly yet. Still holding from ADMD times and still a believer.
Sorry hit send too quickly - they should have started a whisper campaign prior to the event - identified specific target clinics across the country and briefed them on the test patient results with the goal of having them pre registered and signed up to market Isopet in their practices. Then at the conference / during the presentation perhaps or at the booth make the announcement that x number of clinics have just singed letters of intent etc.
Drs love to follow the crowd and HATE being left behind .... we need to create a sense of urgency based on facts, results and most of all bottom line profits for the vet practices.
I think we are missing the marketing piece a little - some people had issues with George but you have to admit - people remembered him and his message! So my advice to Dr. K and his team it s time to find a messenger - a salesman - a showman - a marketer - a translator of corporate capabilities to include patents and how they can be monetized by the masses
Not the PR I would have wanted to see - just being honest - more importantly not enough to entice real investors - it seemed to me to be a message to US - the people on this board / current share holders to inform US that they attended the event / presented data we have all known about for some time / shock a few hands / made new friends etc.
We did not seem to have the "life changing event" moment where the medical and veterinarian worlds were introduced to Isopet and Radiogel as well as provided concrete evidence of efficacy.
No doubt they still have a plan / path forward for commercialization of Isopet and FDA submission but they are certainly missing both opportunities to make an impact on the community as well as burning cash.
To me the most significant piece was their statement regarding what they need to improve - which is - treating the outer limits of the injection areas to minimize the re occurring growth. This is important because this granular level of efficacy is what the FDA will focus on during their approval process. I see this as added line items to the test and evaluation process of the next couple of patients moving forward.
In my opinion the PPS will drop and hover "again" until FDA submission - which should be complete and comprehensive. I do not see massive influx of new buyers / investors because the message is still be shaped and is not ready for public consumption.
On a bright and fair note - since the message is not ready in my opinion for public consumption - the best course of action is to keep a low profile - you only get one at bat with the financial / investment community so they need to have a clear, concise and thought provoking message when they go big and this should include an answer book for ANY potential question either medical or financial.
Just my 2 cents worth - I hold over 4 million shares - I am long - I am honest about how I feel - I believe in Dr. K - one day RDGL will make me a millionaire - time coupled patience and the flawless execution of a well thought out plan are all that are needed
ALSO NOTICE ---- they called it radiogel ..... NOT ISOPET -- wonder why? I am thinking they want to start pushing that name for maybe another group watching....... This is a huge document in my opinion because subject matter experts signed their names to it and put their research careers on their FINDINGS OF FACT.
There may be a little hype before the conference but the best place to make the biggest splash is the conference audience followed by strong press releases. What would bolster the case for ISO PET even more are positive 3rd party industry leader comments / press releases detailing how ISO PET will help them fill a void their have in patient demand and treatment capability.
The icing on the cake would be FDA progress on the human front.
Announcing new applications for ISO PET or RDGL at this point will have little to no impact because they need to first capitalize on ISO PET and find a way to demonstrate to the market they have monetized the technology before any "new" concepts will be taken seriously.
LONG and STRONG from ADMD to now -