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The email on the corporate new Web site does not work yet.
It is on my list to let somebody know it is not active yet.
Keep clinic and corporate number straight
do not forget overseas income
Do not need FDA approval at all
Most likely treating heart patients overseas now
[bhttp://www.bioleaders-forum.com/speakers/kristin-comella]
An updated page, dated jan17
[b Per FIU school site
Was expected to to degree fall 2016
Found a paper by her paid for by FIU
Paper at the essence of stem cell treatments
Prooff????
Research paper while at FIU
While she was getting PHD in Bio Engineering
Here is link to paper
http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0149121#abstract0
compare usrm to ctix
Understand
Look at ctix history, all the way back.
Lot of similarities
Look at details to understand.
short and distort
Pay attention to last paragraphs
http://www.bizjournals.com/boston/news/2017/03/20/an-anonymous-blogger-angers-biotech-investors-but.html
Short and Distort
That is what it is called.
And then
https://investorshub.advfn.com/boards/read_msg.aspx?message_id=18742
Manipulation Alert
https://investorshub.advfn.com/boards/read_msg.aspx?message_id=18742
Throw out BS as fast as you can, hope something sticks
More like a franchise
USRM is the supply chain
Supplies
FDA approved procedures
Study coordination
Patients
Training
Banking
Equipment
USRM First 6 clinics in place
https://nsistemcell.com/locations/
Looks like NSI is the chain of clinics
That is why Comella is listed as CSO
All the videos are the same, just different text.
https://nsistemcell.com/about-nsi-stem-cell/
Look at locations, if treatments catch, they will make a lot of money from folkes who will not want to mess with trials and just get treatments.
Looking at more about clinics...
Then there are overseas clinics to be found.
Success will come from overseas clinics first
Regardless of FDA
This where to look first.
Flags to watch for manipulation
Again... read this
https://investorshub.advfn.com/boards/read_msg.aspx?message_id=18742
All you can do is hold or add if you believe in company
I am a stem cell patient and believe
Count 3/0
Red flag MMM
https://investorshub.advfn.com/boards/read_msg.aspx?message_id=18742
Count 2/0
Mesoblast mass produced generic stem cell boondoggle?
https://www.regenexx.com/did-the-mesoblast-stem-cell-disc-trial-succeed-or-fail/
Read last two paragraphs on disc trial
Repeat
330, gone quick
Reasoning on why
What RMAT Announcement will look like
It will come from us stem cell first.
Then something like this.
http://www.raps.org/Regulatory-Focus/News/2017/03/20/27158/Humacyte-Receives-First-of-FDA%E2%80%99s-Regenerative-Medicine-Designations/
Note, Mesoblast has applied but n9t gotten yet.
Humacyte only one I know off, also nothing on FDA site about any RMAT designation.
Law suit was against eye clinic, not US Stem Cell
More to come, believe me...
Short Vol 50% today
What could possibly be behind this?
Short and Distort
Vol down to 7mil
Shorting vol up to 40%
Two week short interest up 60%
List of news
The long list of new sites that I can not mention
Showed up the day of the Harvard paper.
To just get treated versus a trial
From a stem cell patient perspective
Some just want the treatment and pay for it.
Some will mess with a trial
What do you think the new clinics (oversea and stateside) are all about
Humacyte announced by company
Still looking for how FDA announces.
Maybe it will be left to company
Show me any FDA RATD/RMAT ANNOUNCEMENT
I have not.
Would like to see one to understand process.
All announcements so far by company's
Humacyte on FDA site??
Has anybody found an announcement on FDA
Trying again
Ihub chart way behind marketwatch and big charts
Just an observation
Time stamp on ihub not correct
Verification on FDA CITE
Has and body been able to verify??
I have not been able too, still trying
RATD change to RMAT
look like FDA changed ack..
Just had to get medicine it the title
REGENERATIVE ADVANCED THERAPY DESIGNATION
REGENERATIVE MEDICINE ADVANCED THERAPY
Old bias hard to break
Company info probably in lock down.
Would only expect to see offical public release.
Assumption from all that is supposedly going on.
Article on Stem cell for clinical use
http://downloads.hindawi.com/journals/specialissues/960284.pdf
If you do not think there is a world wide push for the type of stem cell use being discussed.
Real story, FDA overwhelmed by pissed off patients
Hearing on stem cells delayed from last April to september.
Let's hope new FDA head delivers.
http://observer.com/2017/03/fda-nominee-scott-gottleib-rare-disease-drugs/
The coordinated attack on usrm is really a political attack on newly nominated FDA head.
How this affects usrm is to be seen.
If you do not recognize media spin yet......
They will get publicity
RATD was result
What really happened at fda stem cell meeting
https://ipscell.com/2016/09/key-arguments-take-homes-on-day-1-of-fda-stem-cell-meeting/
https://www.fda.gov/BiologicsBloodVaccines/NewsEvents/WorkshopsMeetingsConferences/ucm509279.htm
http://www.patientsforstemcells.org/fda-public-hearing/
http://celltrials.info/2016/09/18/fda-public-hearing/
Could one of the moderators sticky this along with nih paper
RATD designation was result
This is old news and has been going on for years
The Regenerative Advanced Therapy Designation was the result of all this