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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 Eoganachton Feb 25, 2023 11:58am
273 Views
Post# 35305177

RE:RE:RE:New McFarland Labs Research of TLD1433 Processes

RE:RE:RE:New McFarland Labs Research of TLD1433 ProcessesI think it means that they made sure their research doesn't just apply to TLD1433 by also using the PS TLD1633. TLD1633 is TLD1433's younger, more effective and safer brother. McFarland Labs continues ro use it in research even though TLD1433 was preferred for the NMIBC trial. In 2017 TLD1633 was found to be 15X more effective against gbm cells than TLD1433. In 2018  Dr. McFarland explained why TLD1433 was preferred:

"Considering the potency of TLD1633, it may seem odd that TLD1433 was selected instead. TLD1433 was prioritized over the other compound for a number of reasons, including:

(1) there were more synthetic steps required for producing TLD1633, and those steps were low yielding (unoptimized at that time) and required expensive catalysts,

(2) there was more batch-to-batch variability with TLD1633,

(3) the theranostic capacity of TLD1433 was greater (i.e., its luminescence quantum yield was higher), and

(4) we were relatively far along in our pre-clinical studies with TLD1433 by the time the synthesis of TLD1633 was optimized to produce the larger batches required for in vivo studies."


This is just one more example of the vast amount of Dr. McFarland's anti-cancer research Theralase is unable to take advantage of because of a lack of funds.
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