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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 N0taP00pon May 13, 2024 2:23pm
109 Views
Post# 36037284

RE:TAR and other agents

RE:TAR and other agentsTotally aligned with your daydream DJD.  We need something other than the ambiguity on pre-BTD pushouts. At least meet the spirit of the OSC guidelines
DJDawg wrote: Others agents out there for sure. They all have the common theme of frequent repetition of treatment, a pseudo CR that seems good but then when you follow up longer term, a low durable CR.

All this competition talk does create the appearance of more challenges to TLT. But many are no where near being real competition. Adstiladrin's data is more and more unimpressive. IBRX drug requires you to get access to hard to get BCG so that tethers the sales and competition. CGON's drug is biologic so cannot be approved without biologic application steps which would likely lead to early 2026 for earliest approval.

Ideal next steps for TLT would be
- some release at the end of May that shows that they now have longer term follow up data to show even further durable CR. Could even mention that all confirmed by a central lab. These would be good hints that they have the data for the BTD application without saying that they have applied for BTD.
- when they get BTD, it would be nice if they could time some update that shows concrete steps for the phase 1b on GBM. Doing that means that they are no longer a one drug with one use type company.
- that could give quite a nice momentum bump.

Just me daydreaming so far.


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