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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 ScienceFirston May 17, 2023 9:08pm
193 Views
Post# 35453706

RE:RE:RE:RE:RE:RE:What is Pre-BTD Submission to the FDA?

RE:RE:RE:RE:RE:RE:What is Pre-BTD Submission to the FDA?

If TLT was aware of that option (pre-BDT) and that they decided to take advantage of it to put all the chances on its side, then that's very wise as we only have one chance to succeed.

They proved us over the years that they are very attentive to many details and that they never cut corners, never do things superficially.  That's very securing for our investments.

They're taking this very defining opportunity (Breakthrough application) very seriously.

It's just a matter of time.

And an opportunity to add more at these low prices for those that have not yet completed their purchases.


____________

 

RE:RE:RE:RE:RE:What is Pre-BTD Submission to the FDA?
SF, thanks and understood. My point was only regarding the pre-BTD advice submission that Dr Uddin mentioned. I'd never seen that mentioned by the company nor here on the board. Maybe I missed it (very possible). But I'm glad to see that that's a real thing. Sounds like a sanity check with the FDA prior to official BTD application, so as to get advice and not waste a submission errantly.
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