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USRM .09 here we go!
You must be looking at the wrong stock. GREEN!
USRM new hod!! Time to fry shorts
USRM about to break HOD - Pending FDA NEWS
USRM about to break HOD - Pending FDA NEWS
USRM about to break HOD
.10+ very doable today. I agree
USRM watch for green now
USRM ask moving up p/m. Let's burn these shorts.
Gm. Let's see that green squeeze today.
Amazing post! Thank you for clarifying that from an attorney prospective. I was thinking the same thing. If results were not favorable, FDA would have given denial right away. FDA sees favorable data and wants trials to be reactivated to convince them to give the approval.
USRM is a winner here.
Nice rebound from bottom. $80k bidder
USRM $80,000+ bidder now
I will keep buying. Thank you for the advise.
Time to buy more :) at least for me
L2 now insanely thin. All .001 buyers are out. Time to go green
More millionaire made from penny stocks than anywhere else. USRM most likely make more
USRM let's see that squeeze into .25 then $1+
NOUV 100% in buys and climbing.
NOUV 100% in buys and climbing.
NOUV 100% in buys and climbing.
USRM steady accumulation now. HOD coming up
USRM has received reactivation status of the MARVEL phase II/III trial." !!!!!!!
That is very big news
USRM from FDA WEBSITE :)
https://www.fda.gov/BiologicsBloodVaccines/CellularGeneTherapyProducts/ucm537670.htm
As described in Section 3033 of the 21st Century Cures Act, a drug is eligible for regenerative medicine advanced therapy (RMAT) designation if:
The drug is a regenerative medicine therapy, which is defined as a cell therapy, therapeutic tissue engineering product, human cell and tissue product, or any combination product using such therapies or products, except for those regulated solely under Section 361 of the Public Health Service Act and part 1271 of Title 21, Code of Federal Regulations;
The drug is intended to treat, modify, reverse, or cure a serious or life-threatening disease or condition; and
Preliminary clinical evidence indicates that the drug has the potential to address unmet medical needs for such disease or condition
...
If the RMAT designation request is submitted to your IND as an amendment, the cover letter should specify that the submission contains a REQUEST FOR REGENERATIVE MEDICINE ADVANCED THERAPY DESIGNATION in bold, uppercase letters. If the request is submitted with an initial IND, the cover letter should specify that the submission contains both an INITIAL INVESTIGATIONAL NEW DRUG SUBMISSION and REQUEST FOR REGENERATIVE MEDICINE ADVANCED THERAPY DESIGNATION in bold, upper case letters.
With Reactivation FDA can grant RMAT :) we are golden!
"THEY CANT GRANT RMAT UNTIL THE TRIAL WAS REACTIVATED!!!!
RMAT DESIGNATION COMING IN DAYS"
We got the reactivation !!
USRM $30,000 in buys now
USRM expect more revenue & profit with FDA APPROVAL
$100,000 bids. Someone still adding
If she breaks .10 now OMG! Going to go much higher. Beautiful shake and rebound
CSTI CDEL NITE all main bidders now. GREEN TIME!
CSTI done selling. Moved to .19
Current trial looks favorable by FDA. Hence why they reactivated it
That trial has nothing to do with current TRIAL.
USRM $70,000+ bids. 90%+ buys. Awaiting FDA APPROVAL
USRM $70,000+ bids. 90%+ buys. Awaiting FDA APPROVAL
USRM over $70,000 bids. 90% in buys
USRM $60,000* bid
USRM more new highs
USRM HOD!
Mostly all buys so far