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I agree with you and think it’s been great hearing these updates with isopet. This kind of move for isopet has been way over due.
More clinics getting trained and approved to use isopet just makes it easier for people to get to clinic and actually get to use isopet on their pets. I’m sure with the 3 clinics they have already they had plenty of interest but more than likely to far away and expensive to travel to the clinics.
Most people will do just about anything to try and save their pets but most also know there’s a limit as well unfortunately.
This isopet news is great, about time they are expanding.
I can see that happening
It’ll happen, when who knows.
They get ide approval this will move pretty high then come back down and settle in probably around a $1.00 maybe a bit higher.
Also as they get more clinics set up for isopet more revenue will come in, but that will take some time to build a constant revenue stream
Who knows a buyout could happen anytime after ide approval.
$5 within the next year is very doable.
The Doctor definitely does not spew bs daily.
He doesn’t put anything out until he’s fairly confident on the progress. Granted there’s been delays and what not that he should have let the shareholders known a lot sooner. Oh well.
So don’t get discouraged when we go weeks sometimes months without hearing anything.
What news
Missed this. This is great news. More clinics means easier access for people to take their pets to get treated.
From radiogel on Twitter.
Once we've received our IDE approval from the @US_FDA to begin human trials, we will be attacking #ThyroidCancer. #RadioGel™ will be offering a new progressive process. Having Mayo Clinic Doctors assisting with our application process has been invaluable.
Once we’ve received our ide approval.
Very bold optimistic statement in my opinion.
Interesting tweet this morning with a pretty bold statement.
I would have to say that the doc has something up his sleeve, just waiting for the right time to release it.
He’s dealt with the fda many times before in the past. So I truly believe when he’s ready to release information it will all be good and things will move fairly quickly.
A lot faster then a few on here believe will happen.
The tweets about isopet, it’s not so much about building the business. It’s about collecting data. More patients more data more proof especially if they can treat the tumor at an early stage. That’s what the fda what’s to see. Data. And if it happens some of the more rare and harder to treat areas like the brain etc…. It will be easier to get approval for those uses down the road.
So saying that isopet isn’t that big of a deal. Guess what it’s huge deal when it comes to collecting data. On animals radiogel can be used every where. ????
I didn’t say indications, I said other projects, meaning other uses for the gel other than delivering the Y90.
Honestly once ide is approved what will the doctor be doing, the Mayo Clinic will be doing all human testing, he might pop in every once in awhile. So why not start working on other uses for the gel and it wouldn’t surprise me that he starts animal testing on some of the even harder area to treat cancers, like the brain. Because once they thyroid is approved every cancer below that will get approved fairly quickly.
Yes we have a long way to go but at the same time not really. Unfortunately way too many unknowns at the moment to even guess when it will finally come together, it could happen before the end of the year or it could be spring. Guess we will find out soon enough.
Lol I guess so, maybe some of them need to get their eyes examined.
I see it as a positive as well and I see it as something they have already done and they will keep on tweeking the product and technique to benefit in other areas of medicine.
Pretty sure the tweet is just stating they have made adjustments over the years to benefit the company and patients.
Am I missing something on that tweet or are these guys blowing this tweet way out of proportion
New techniques may lead to new patents.
Doesn’t say new formula. ?????
Besides anyone that follows biotech knows that they will be trying to make as many uses for a single product, more options for different uses equals more money.
Remember the tweet before that involved the offering. The money was raised for the forgoing year for animal tests, project and isopet.
When they come up with something new who do you think they will test it on first. ANIMALS.
So some of you are going out on the deep end for no reason. Man it must be stressful.
All they did was state what they have been doing the last couple of years with the product. It doesn’t state they have been making changes to it to date.
If it does point it out. You all are over analyzing the tweet.
Guess people are tired of waiting and or need cash.
As far as I know there’s been no information released on how many procedures have been done in the second quarter.
I think the doctor is done announcing every procedure being done unless it’s
treating a new area, liver, pancreas, etc…
I’m with you it would be nice to hear what’s going on in Long Island.
Welcome back
Ticking time bomb, tik toc
My guess is people think they have months to accumulate and or buy back in before big news drops. Considering they have to submit the plan then the fda has to review it and then a meeting with vivos.
Then if plan approved the test can start.
Which in my opinion once the plan is submitted things will Move fairly quickly to get the test started.
As for animal testing. The fda called for one test not more than one, granted yes they can ask for more if they aren’t happy with the information they received from the first test. Highly doubt it but possible.
In the docs message animal testing, just animal testing nothing stating that the animal testing is for the ide.
hmmm they literally have a blue print now with what the fda wants to see from the animal tests.
So I’m guessing and only my opinion, they will start animal testing (plural more than one test). On the next cancer they would like to see get approval, more than likely the brain or another very difficult organ to treat cancer in. The doctor has always wanted to have something to treat kids type of cancers especially in the area of the brain.
So in my opinion they will do more animal testing in a harder to reach area. They will also keep improving their patent protection especially overseas. They will also explore other possibilities for the gel as well work on expanding isopet.
My opinion of course.
Money raised is for the forgoing year for isopet and other projects, nothing said about funds being used for ide and or test for fda.
Meaning they have the funds already for the fda test and ide, they raised money to expand isopet and other projects. ?????
There was no doubt that they had the funds, the doc stated that. Even before the offering he said they had enough cash to get through ide.
I myself have stated several times that the doc had it under control and if needed to could get the funds. A statement the doctor has made a few times.
But now it seems like vivos is In the hands of the fda, so it sounds like they are moving forward with more expansion on isopet clinics possibly. This will be interesting to see what happens they had a lot of interest over in Europe with isopet but were waiting until Vivos was farther along with their ide submission.
My opinion in the coming weeks we will be getting some much needed updates across the board.
I thought we banned that name from ever being said again. Nightmares oh the nightmares
Coming through with a bulldozer
The thing is you don’t have a clue what it will cost to do human testing. You do realize this is for a device, meaning half the patients needed or less plus have the time meaning less money needed.
The doctor has stated they had enough funds to get ide.
Besides they already stated they had enough money on hand to get ide.
So that’s telling me that they did this to make sure they had cash on hand to start phase one testing as as ide is approved.
Can’t do much with a approval if you don’t have funds to move forward.
My opinion of course, probably here something within the next two weeks maybe sooner.
It is also on otcmarkets, I didn’t look at the filings at first, My bad.
Thanks
Where did you see this. Otcmarkets hasn’t updated and neither has tdameritrade
Still sitting around 343 million shares on those sites
Makes perfect since.
Just my opinion but look for a buyout around phase 2 or 3 human testing. Long time ago the doctor mentioned selling to someone that can take this to market quickly when approved.
So honestly I wouldn’t worry about it and just see what unfolds after human testing starts.
I would like to see that as well, then they could use the money that they raised for expansion/advertising.
Guess we better get through this test and actually ide approval before we worry about that.
Well if the outstanding shares weren’t almost maxed out at 3.8 billion shares and the authorized shares were actually around a few hundred million shares then this would more than likely be at or around$.50 cents or higher but with this share count it’s going to be pretty tough to get this to .05 cents or higher and actually stay there.
Hmmm just my opinion here so they lower the offering, so did the ones with deep pockets convince the doctor to lower the offering and by doing so they will buy into the offering as soon as they get the results from the test.
Which we all know will meet and or past the expectations of the fda. My opinion the fda likes the results of the test it will be a thumbs up for ide approval.
So a possibility of them closing out the offering before ide approval is pretty high and would give them the cash for human testing at least for phase 1.
My guess with the satisfactory test results the share price will start moving up before ide approval.
Not knowing the cost of human testing which I wouldn’t think it would be all that much considering that the testing length per phase will possibly be reduced considering the life expectancy of the gel and Y90 in the body.
So I guess we will see what happens.
A lot more going on that we don’t know
Ha
I believe the fda will follow through and expedite everything like they said they would so it’s just a matter of the doctor finishing up the plan which I believe they are getting close, why send out that tweet otherwise.
If it’s a true expedite, the review of the plan shouldn’t take long at all. As long as it’s the same board members.
Now it all really depends on this expedite. We all know what means but how fast will the fda actually move on it.
Time will tell. Wouldn’t be surprised if the plan review with the fda happens within the next week or so.
I’ll have to say that’s probably worse case scenario.
Nope there using american rabbits
Agree ??