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Personally, I think our monster heart results news comes out within the next 9 trading days and possibly only 4.
Even if I have to force it out. ;)
Yep...didn't mean to do the first one. On my phone and can't edit.
Texas Heart Institute acknowledged that the article that JoeCanada posted yesterday was done in their lab. Which is "supposedly where our heart prevlinicals are being done according to some serious research I've done. Looks like that was 100% ENDV.
The @asaiojournal paper is recent work from our Stem Cell Engineering Lab and UH: https://t.co/iTAakDtIWf
— The Texas Heart Institute (@Texas_Heart) May 26, 2017
Another nice day tomorrow, then a 3 day weekend and big news next week would be just perfect!!
I thought Rabbits were at Texas A&M
People don't know about our square wave patent. They're waiting on a PR.
And tissue. Plus diabetes I believe.
....and there are our trial results. Successful!!!
Are you kidding? I'm happy as hell that I've had this much time to accumulate more than my initial buy in amount. It's not if, it's when. The answer is very soon.
Won't effect financing at all. Results are 100% what financing is based on.
Yep, got me another chunk as well. Hard to pass up .058's!
Not really anything to talk to them about. You get the same answer.
"If it hasn't already been released as news, any new information will come out in an 8-K or a press release.
It's a little bit more than that. When you search for stocks on Google, I hub is the first thing that comes up. So there are tons of new investors checking this site out daily. We don't need crap like he's posting. That's my problem with it. It's not a matter of whether I can see him or not
Anybody been watching today's 1000 share buys...if they're even him today.
I wonder if someone is faking 1000 buys now pretending to be him to keep this from going up?
I'm kind of digging his crystal ball seeing as how my funds don't clear until tomorrow.
I'll pick up ALL the .044's and then we can be on our way!!
Exciting sh*t!!!!
Just shows how manipulated this has been lately. When it's left alone, it moves so easily!
No, not just 1 trial.
Sorry man, I drive most of the day and don't have time to go in depth at this red light....lol.
I'll try to message you later today to answer what you asked. Impossible for me to do it right now.
Just to be clear, diabetes will take a long time to finish after your trials. What I meant was we can get FDA trial basis designation, which means we can send our product to market on a trial basis while they are still testing it. That's what I think will happen with diabetes. The rest will be approved within my timeline in my opinion.
7 months until end of 2017. Another 3-4 months considered early 2018. So that's just under a year from now.
We will get FDA fast tracked for some if not all of what we are in right now.
FDA will take max of 6 months after that....fast tracked can take half the normal time.
This is what I think we are currently in and about to get results from in the next few months...Heart, liver, tissue, bone.
Diabetes will take more time but we might also get the FDA trial basis to market designation.
We now have Critical limb Ischemia and NASH starting clinical trials.
So between heart, liver, tissue, bone and diabetes....I think it's possible with our funding (soon to be in place with clinical results), for us to have most and if not all of those first 5 at least finishing up, if not complete by April 2018. Just my opinion but that's how I see it. They are getting FDA orphan drug applications filled out as we speak, I guarantee.
Maybe as far as you know, but not as far as I know, imo.
By early 2018, we should have 4 or more FDA approved treatments ready to hit the market. Some of which will be life changing opportunities for many people.
It could be earlier than that if the FDA grants us one of their fast track designations (orphan drug, investigational device, etc..).
Not only that, but we keep on adding stuff into our pipeline with Critical Limb Ischemia and NASH getting ready for preclinicals.
It's a perfect set up!! We should get results of up to 4 preclinical results and soon after, FDA trial info. And in between those 2 things, our private funding deal will get finalized!
We have a lot of news coming starting right now and through the next few months. I'm not sure if they'll do each trial as they finish, all at once or stagger them. Either way, we are going to be a BIG deal very soon!
Lots of comparisons to Pulse in here.
Read this article. Even though it's biased, it's factual. We are world's ahead of them in technology, patents and device ability.
Endonovo Therapeutics is to Pulse Biosciences,
what Arnold Schwarzenegger is to Richard Simmons.
https://seekingalpha.com/amp/article/4070956-pulse-biosciences-inc-high-voltage-hype-set-short-circuit
Well, with all the trials we have going on, there's no way we get bought for our market cap price when we hit $250M, imo.
Way too much value coming down the pipeline to settle for that amount.
I personally think we are going the licensing royalty route until a BIG FISH comes knocking with a price we can't refuse in the double digit billions.
In my opinion, we should be getting a cluster of multiple finalized clinical results between now and end of 3Q.
3 or 4 different results if my count and DD is correct.
Between now and the end of summer, we should be getting HUGE news event after HUGE news event!
It would be a shock if we weren't at $1 or much much more before Halloween.
These events are finishing up and are getting aligned for release over the next few months. The ride is getting ready to start....claim your shares now or forever grit your teeth!
I've been adding the whole way since my initial core purchase in March. I've bought as low as .04 and as high
as .11 and I'll be adding again later this week and will continue to add every chance I get at these prices.
Plain and simple....you don't keep putting your device through clinical trials and paying millions of dollars to test it, if it's failed previously. Since it's basically the same device, conceptually, for each treatment. If it fails one, it'll likely fail them all. If it's successful at one it should in theory be successful in all.
The fact that Mr. Michael Mann is buying shares hand over fist.
Combined with the fact that they are starting up a brand new batch of clinical trials (NASH and Critical Limb Ischemia), should tell you everything you need to know about how the previous clinicals are going (or how they went).
I know what I believe is happening.
Yep, I totally agree!
I've been doing a ridiculous amount of reading this weekend. Articles, write-ups and PR's from early 2014. Piecing together information about the technology, FDA applications, Orphan Drug designation, Investigation device exemption, many preclinical trials and how long it typically takes for any and all of this to take place or finish with results.
I have a much better grasp on where we are and what to expect now, than I even did just 48 hours ago.
We have some BiG news coming, as the timeline tells us from as far away as a year ago. That big news might be enormous if everything went as planned.
FDA "privileged status" is in our near future imo.
This is a "not paid for" article, written 7 months ago but gives good insight into where things are heading and time frames for certain approvals as well as what's next.
http://www.microcapdaily.com/the-inside-scoop-on-endonovo-therapeutics-inc-otcmktsendv/116750/
Every time I read an article like this, it does 2 things.....blows my mind that we're trading in the .05-.07 range with a $15M market cap AND makes me realize what a freaking STEAL getting shares at this price are and how lucky we are for this brief period of time to be able to accumulate as much as we possibly can before they're much more expensive!!
You got your wish. ;)
https://twitter.com/endonovo/status/866002050655502336
Well, there are professional athletes currently using the previous device as we speak. If it weren't beneficial, I don't think they'd use it.
This device was originally designed for NASA astronauts to treat themselves in space for injuries. So it's exactly what it's for.
This device was being sold for $600 before Endonovo acquired the patents and Dr. Rudd advanced the technology and its ability to what it is now, which according to Dr. Rudd and Alan Collier, it's "vastly superior" and "far advanced" over those models that were sold.
I have no idea what Endonovo plans to do or what any BIG company who buys us out plans to do. But these devices could be sold as OTC devices, prescription only devices or used as inpatient treatment/therapy devices only used in medical facilities by medical staff.
Either way, the sheer volume of people in the world multiplied by the amount of patented ailments, diseases and injuries that this device can cure, heal or strengthen, makes this an amazingly valuable device and asset combination to own for ANY company! Multiple billions should be the bare minimum!
All I'm saying is why would t you use the best possible technology?
Would you rather it cost less and be healed in 6-10 days or pay quadruple and wear a cast for 8 weeks?
This is a smaller, less important benefit of our technology...just pointing out its abilities.
That's why they have to go through clinicals first. You can't "manufacture and sell" a medical device that hasn't been tested and approved.
Dr. Rudd invented the new technology in the new non provisional patent that was PR'd at the end of March 2017, to treat organs and tissue. Supposedly it's far advanced over the previous device according to him. Which was already far advanced over anything currently available in the medical world. Once the heart results come out any time now, this will become a whole different stock and company.
I've said all along (and it's just my opinion) that I think they have a strategic entry plan into the medical device world.
Broken bones aren't looked at (by FDA & Big Pharma) as life changing to have them heal faster....that's just a benefit of our device.
In order to get our device and patented treatments out there and out there faster, we need to run trials on things that are either life saving procedures or are treatments for very rare diseases/illnesses where our device is superior to the current and best out there.
Spending money on pursuing bone healing is not going to bring much recognition, which is currently what we are looking for.
We want to break into the news with a heart cell healing ability device, post cardiac trauma. Something that can only be half assed treated right now with pills that have bad side effects.
When we get results that we can completely regenerate damaged heart cells, non invasive lay and without any side effects.....it's going to be ON!!
Dr. Rudd's old business called We Heal Animals was basically just that.
There's a video of Dr. Rudd talking about a dachshund that jumped off of a bed and broke its back. The family built a little wagon for his back legs to fit it so it could pull himself around. The dog did that for over a year but the family felt like his quality of life was suffering and were going to put it down. One of Dr.Rudd's salespeople happened to be in the vet that day selling his device. He asked the family if they'd be willing to let him try the device on their dog, they agreed. Long story short.....10 days later that same dog was running around in their backyard good as new.
It's a good video/interview of Rudd. It was posted here. I think I saved it. I'll PM it to you if I find it.
I read a huge article strictly about bone breaks. In the USA alone, there are 5M bone breaks a year. Non surgical bone breaks of (shoulder, patella, leg, hip, hand, ankle, forearm, foot and fingers) average cost is slightly over $2,000.
That's $10,000,000,000...$10B in non surgical bone breaks that take 6-10 weeks to heal.
In surgical breaks, the cost multiplies by 5-15X the cost!! $50B-$150B annually!!
TVEMF can not only change how fast you can heal. But how inexpensive comparatively it will be for your insurance company.
So not only can ENDV take over a potential $10B annual non surgical market. But could also convert a portion of that $50B-$150B market of surgical breaks into potential non surgical breaks. Let's just say that only 10% of surgical can become non surgical using TVEMF. That would be one an approximate $10B market (10% of $100B surgical breaks).
That right there is a $20B annual market where we can takeover and heal patients 80-90% faster and less expensive.
Even worst case, no surgical breaks can be saved. It's still a $10B section of medical costs that we can take over. This is only in the US!!!
This is just 1 simple ability of our device, and only comparing it on a very specific non surgical break portion of USA medical costs, using a portion of just 1 of our patents and yet we can take over a $10B market and drastically change how bone healing is done.
You think ENDV isn't going to get bought out eventually for an INSANE amount of money!?!?!
Just add in the rest of the patents (Heart, Liver, Diabetes, Sickle Cell, Kidney, NASH, Stem Cell, etc, etc, etc...)
And then multiply it by the number of patients needing it IN THE WORLD...not just the US like my bone break cost was done.
The ENORMITY, of our POTENTIAL and VALUE, is IMPOSSIBLE to wrap your mind around. I don't think many people get it quite yet.
Nice article find Joe!! Hadn't seen that one before.
I copy and pasted the first few sentences of that cut off article into google search. Nothing came up for it...BUT...a ton of other articles did. Some interesting reads. Most are pretty old though. But it's really cool to see that ALL of the technology that was developing back then, we have a far advanced version of and full patents to cover it. We are in the fast lane and will be blowing by everybody very soon.
Right.
Because he hasn't been buying every day for the last year plus.
This is "clearly" his "new" plan. He just decided to start doing it a year in advance of this day.
How are you so smart?
Check this out....We've got most of this covered and we are light years ahead of current medical treatments on them as well...
"The world's superpower doesn't rank where you might expect it to. The United States scores an 80 on the index, which is at the bottom of the second decile and puts it on par with Estonia and Montenegro.
The United States measures well for diseases preventable by vaccines, such as diphtheria and measles, but it gets almost failing grades for nine other conditions that can lead to death. These are
-lower respiratory infections,
-neonatal disorders,
-non-melanoma skin cancer,
-Hodgkin’s lymphoma,
-ischemic heart disease,
-hypertensive heart disease,
-diabetes,
-chronic kidney disease
**And the adverse effects of medical treatment itself!!