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Theralase Technologies Inc. V.TLT

Alternate Symbol(s):  V.TLT.W | 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 CancerSlayeron May 04, 2023 3:55am
236 Views
Post# 35429263

RE:RE:RE:RE:RE:one article - new today

RE:RE:RE:RE:RE:one article - new today

Correction has been highlighted:

It looks like they are taking a more cautious approach in terms of promotion/getting the word out.  You probably don't want to oversell potential on relatively limited trial data pre-BTD...jmo. 

There needs to be an effective option that not only works, but one that is patient-friendly, doesn't break the bank & can be more easily accessible (i.e. more easily/efficiently manufactured).  It's such a shame that in this modern era so many thousands of high-risk patients aren't even receiving the standard of care (SOC or BCG).  Patients are being cut off from the SOC,  receiving a lesser dose of the SOC, or not receiving the SOC at all due to the BCG shortages, which are expected to last for years.  Someone at the FDA or higher needs to finally put patients before profits...we are all patients.

Our time will come...the FDA can't ignore the fact there are still so few FDA-approved options, all of which are expensive, treatment-intensive & have demonstrated fairly suboptimal efficacy.

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