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Theralase Technologies Inc. V.TLT

Alternate Symbol(s):  TLTFF

Theralase Technologies Inc. is a Canada-based clinical-stage pharmaceutical company. The Company is engaged in the research and development of light activated compounds and their associated drug formulations. The Company operates through two divisions: Anti-Cancer Therapy (ACT) and Cool Laser Therapy (CLT). The Anti-Cancer Therapy division develops patented, and patent pending drugs, called Photo Dynamic Compounds (PDCs) and activates them with patent pending laser technology to destroy specifically targeted cancers, bacteria and viruses. The CLT division is responsible for the Company’s medical laser business. The Cool Laser Therapy division designs, develops, manufactures and markets super-pulsed laser technology indicated for the healing of chronic knee pain. The technology has been used off-label for healing numerous nerve, muscle and joint conditions. The Company develops products both internally and using the assistance of specialist external resources.


TSXV:TLT - Post by User

Comment by N0taP00pon Feb 05, 2023 3:42pm
325 Views
Post# 35267854

RE:My rough math with assumptions

RE:My rough math with assumptions I would also expect that they would attempt a 5 to 1 split if the stock holds steady above $1 after BTD.  Then list it on the Nasdaq and raise money much more easily. Then negotiate for a JV or sale from a position of strength. The BTD golden buzzer needs to go off on-time first
N0taP00p wrote:
The total BCG resistant NMIBC opportunity is estimated at $1.1B to $5B annually (corporate presentation).  Assume 300M shares (options and warrants inclusive) and assume a conservative opportunity of $1.8B, give or take, after BTD approval. I'm assuming the other 60% of the available max of $5B will be split between newly-approved or in-process trials. Then apply a conservative valuation of 1X of sales. That would put the stock price in the $6-$7 range, if my math is right. That's a nearly 3000% rise from current levels, over a period of UNKNOWN time.  All with one indication and without considering other opportunities as a combo drug with immunotherapy and gene therapy. The experts here can hopefully fix any major gaps in math.
 
So the big need is for the clinical data to be so undisputably good that this treatment becomes the de-facto for BCG resistant NMIBC. To be considered for more upstream use (before trying BCG - as a standalone, or  in combination with already approved drugs like BCG or Keytruda) might take a while, give how cautious the FDA is of late.  IMHO.   


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