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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 Bigkahuna57on Sep 14, 2024 1:24pm
507 Views
Post# 36223897

More Than $7 With Combined Indications

More Than $7 With Combined Indications@2b7f6fab & DX33, et al. 

You both make great points and I might add that if/when TLT inks several license agreements the SP should easily move above $2.5B. A few general estimates being: More outstanding shares than the end of this year b/c the license agreements/partnerships are hopefully within the next year. I think any partnership must be based on trial performance of NMIBC and/or whether Roger permits (outside partner) initial lab testing that would require NDA's and time to develop the "combination" proof-of-concept outside of TLT's lab results. A $300-500M upfront front deposit w/annual license payments would easily exceed $1B after FDA approval for any "combination" cancer drug therapy. Virus vaccines would be additional too.  The annual spend for each indication/market segment for virus or specific cancer treatment seems plausible. Any partner would already have the R&D cash allocated for immediate investment. The recovery time from initial investment would be quick (3-5 years). The "data" for the FDA is the end of the obstacle course. FOMO, desperation, greed and/or shear self-preservation for any of the companies featured in the Merk article will initiate the negotiations for licenses and partnerships. I think the independent testing of combinations with TLT1433 is the reason for the 2025 timeline. On to the "realists" who bellow to the board.

To any of the "other" "realists" on this board - Do keep in mind that TLT does not have control of the patient follow-up data that the FDA required since the Pre-BTD meeting/review. You somehow keep bellowing to the board that TLT has no expertise in execution. Yet none of you appear to have any memory of the FDA requirements. Or purposely care not to remember correctly.  How can this be with you decades of experience developing the cure for cancer?  "The Group of Realists" preface your complaints/statements of fact without the inclusion of the FDA requirements, which are the highest order of precedence in this process. Every time you bellow (to each other) the rest of us recognize your hollow attemp at an argument to discredit the executive team. 

I can only guess as to why you're hear. Cui Bono? Clearly - not you. If not you, then who?

I appreciate the many contributions of those with whom I share the hope of a cure for cancer and vaccines.  

GLTA.
Regards, BK.
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