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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 CancerSlayeron Sep 05, 2024 7:18pm
136 Views
Post# 36210862

RE:RE:RE:RE:RE:RE:General question for the board

RE:RE:RE:RE:RE:RE:General question for the board
Glad you brought that valid point up...

CG0070 requires treatments spanning almost 2 years, & there's an expanded cohort (US & Japan) that would receive maintenance treatments for up to 3 years...it's kind of like getting endless booster shots in order to keep the immune system triggered/awake.  The fact that so many doses are required in this protocol, my guess is that once you stop dosing, immunity will wane thereby increasing risk of recurrence.  
Additionally, such extended treatments impose an intense burden on patients, docs & the overall healthcare system, which makes this endless treatment course expensive & less practical for many.  

As you suggested, the more interesting/telling data will be the durable response rate "after" all treatments have been stopped.  The "pseudo-CR" will then show its true colors.  It's also somewhat a "pseudo-comparison" when one compares two different classes of drugs, which is the case when comparing our ACT with CGON's.  

People need to understand that just because a drug may be best in/across-class, doesn't mean it's the best option for patients & the healthcare system.  

The FDA clearly understands this when considering the nature of this unmet disease & FDA's prior approvals.  JMO..
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