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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

Post by ScienceFirston Dec 05, 2022 9:23pm
318 Views
Post# 35152388

Valuation

Valuation

We all know that a catch-up in market valuation will come soon.

Oncology stocks, once valuation is unlock, get the highest valuation of any medecine fields.

Just to show how undervalued we are at the moment, Belly's Pharma, which is only a one-indication stock (A Leader in the Development of The Novel P2X3 Antagonist Class Targeting Cough and Other Hypersensitization Disorders) and is expected to be granted FDA approval, is now valued at 1.7B$CAN.
 

Our turn is soon coming.  We now have clinical data to apply for FDA designation(s), CR% and DR% superior to Keytruda, low side-effect treatment, high QOL treatmen, low number of treatments, management that has put their own money into the stock, that also participated in 2 pps and have been granted stock options and we have a "commercial revenue (projected)" milestone that is planned for early 2023 and that seems to be associated to a potential Accelerated Approval program, plus a FDA's response planned approx. around late February for the Breakthrough Therapy designation.  And an industry that has guidelines on how much pivotal Ph. 2 data can be worth.  Not to mention a 2nd PDC (Rutherrin) that is more potent than our current PDC (TLD1433) and that aims at 2 tough indications; NSCLC and GBM.

Valuation should start kicking on granting of FDA designation(s), possible jv offer, etc ...




 

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