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Theralase Technologies Inc. V.TLT

Alternate Symbol(s):  TLTFF | V.TLT.W

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 Donein25on Apr 24, 2024 5:38pm
181 Views
Post# 36005981

RE:Anktiva plus BCG Durable CR numbers

RE:Anktiva plus BCG Durable CR numbersthanks for the insightful break down Eoganacht. What I also find interesting is that they got approval with just 77 evaluable patients. That is significant because FDA apparently allowed them to just follow the 77 patients 3 years out. 

I would think TLT would be given the same type of consideration for possible AA, at or below 100 patients; meaning no new confirmatory trial;  follow our CR patients for 3 years.

If you look at the most recent TLT Corporate Presentation it mentions under Study Design: "Patient followed up quarterly for 2 years and then semi-annually for 3 years". That 2 yrs/3 yrs follow up has never been disclosed before (that I can recall) as part of the study design.  I have faith that this new study time frame is a directive from FDA that we can obtain AA in the coming year or so and use the follow up 3 years as our confirmatory obligation to full approval.
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