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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 Maxcitracon Dec 18, 2024 12:09pm
164 Views
Post# 36368190

RE:JV with Merck's Keyteuda a bad idea...

RE:JV with Merck's Keyteuda a bad idea...I like the $200.00 target price, Theralase will get there one day.

As for immunotherapy, TLT compound(Rutherrin) work with Immunotherapy as specified in this link.
2024-06-18 | Rutherrin(R) Increases Efficacy of Immunotherapy Preclinically | TSXV:TLT | Press Release

And immunotherapy market is approximately US125 Billion a year, and Theralase will certainly one day grab a chunk of it.

gojotv! wrote: When business hounds try Science, crazy ideas abound. I'm reading here that some want to JV with Merck and "combo" Ruvidar with Keytruda...
The idea doesn't work on so many levels.
First, Keytruda is an immunotherapy, where Ruvidar is a targeted cancer killer.
Second, Keytruda's patent expires in a couple of years, before Ruvidar's usefulness in other cancer therapies can be fully developed.
Also, Keytruda has toxicities which Ruvidar aims to eliminate from oncology.
And most of all, Ruvidar is currently being tested in a "two treatment" protocol, which limits our results. In the real world, patients will be able to get Rividar until their cancer is destroyed - any time after the first treatment. Can you imagine how our "partial response" patients would do after 4 or 5 treatments? They'd be cancer-free, IMO.
So, enough with the crazy talk, let's aim for "Ruvidar - exclusive" treatment protocols, and a $200 share price.
And that is all.
Happy Holidays!




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