Replies to post #39941 on US Stem Cell Inc (USRM)

[mtlebomac]

Good to see you here Camelot!

Good luck my friend!

USRM$$$

[Kramden1]

Yes sir we do!

[legalizeMJ]

"Why is USRM running"? " What catalysts are causing this?"
The 21st Century Cures Act was passed by Congress and signed into law,
following the passing of the 21st Century Cures Act, U.S. Stem Cell, Inc. has applied to the FDA for Regenerative Advanced Therapy or RAT Designation.
1)
http://investorshub.advfn.com/boards/read_msg.aspx?message_id=129709762
Quote:Finally, footnotes from recent pacer filings involved with the Northstar mention buyout OFFERS.

FDA RAT approval=ANY DAY NOW.

USRM will be above $12(twelve dollars) per share right after FDA RAT approval.
2)
====CEO's BLOG====: USRM has applied to the FDA for Regenerative Advanced Therapy or RAT Designation.
http://us-stemcell.com/ceo-blog-u-s-stem-cell-inc-is-off-to-a-great-start-this-year/

Quote:As we recently announced via 8K, we are also working with General American Capital Partners (GACP) to open 10 new clinics in the U.S. called Stem Cell Centers of Excellence. We are excited to help GACP provide stem cell services to new patients in a variety of metropolitan areas over the next three years. In addition, we have entered into an agreement with GACP which will allow for growth of the tissue banking facility. Read more about the agreement with GACP here: https://www.sec.gov/Archives/edgar/data/1388319/000118518517000536/usstemcell8k030817.htm

On regulatory news, following the passing of the 21st Century Cures Act, U.S. Stem Cell, Inc. has applied to the FDA for Regenerative Advanced Therapy or RAT Designation. Thanks to the REGROW component of the Cures Act, The FDA will grant RAT designation for a regenerative medicine therapy that is intended to treat, modify, reverse, or cure a serious or life-threatening disease and demonstrates preliminary clinical evidence that the product has the potential to address unmet medical needs for a disease. We believe that our MyoCell® product meets these requirements as we have demonstrated clinical efficacy in both preclinical and clinical studies including our most recent MARVEL Phase II/III trial. If RAT designation is granted, this could expedite the approval process with the FDA. More information on the FDA’s new RAT Designation can be found here: https://www.fda.gov/BiologicsBloodVaccines/CellularGeneTherapyProducts/ucm537670.htm

3)
USRM's revenues, profit
http://us-stemcell.com/u-s-stem-cell-releases-positive-2016-financial-results/
4)
FDA Approval is FOR SURE because FDA CAN'T work against Congress(FYI: The 21st Century Cures Act was passed by Congress and signed into law).

$$$$$$$$$ Go USRM $$$$$$$
The above post is my own opinion. Do your own dd before buying/selling.