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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 Oct 28, 2024 3:46pm
195 Views
Post# 36285618

RE:RE:Sorry wrong Link last post :-(

RE:RE:Sorry wrong Link last post :-(
wildbird1 wrote:


Oden6570.

In the article you provided there is a sub-article.

Sample page for NMIBC Market Outlook Report

It is mentioned that in Japan Adstiladrin is expected to capture the largest market shares for BCG resistant patients.
From what I read on this board Adstiladrin is a repeated treatment has contraindications and has a much lower CR% at 450 days than TLT treatment.
Adstiladrin is absolutely not in the same class as TLT treatment.
Let's be clear on something Japan is a very very small market, but that is not the point, the point is that if Adstiladrin is the best treatment they can offer to BCG resistant patients, then there is an urgent need for a better alternative like TLT treatment.

The same apply to other much bigger market like US.





In the US, it has been reported (per a web-based survey of urologic oncologists) that intravesical Gem/Doce (chemo) is also commonly used as a first-line bladder-sparing treatment (BST) for BCG-unresponsive NMIBC.  However, there were significant obstacles reported to prescribing this treatment, which included clinical workflow issues (i.e. frequent dosing = 6 weekly doses, followed by monthly maintenance), challenges with supply & cost.

Re: Adstiladrin, it had a 12 month DOR rate of 24% (vs our ~27% 12 month DOR rate, which has potential to increase).  As a viral vector gene-based therapy, Adstiladrin cannot be used in immunocompromised/deficient patients & has special handling requirements (frozen suspension with specific thawing requirements).  It also requires more treatments than our ACT....from what I can gather, a complete treatment course would involve a treatment every 3 months for up to 4 years.

In August 2023, a global group of bladder cancer experts made recommendations (which were updated) that includes the above two treatments as the currently preferred first-line (non-BCG) bladder-sparing treatments.  There was one additional recommended BST that included BCG as a combo treatment.

So, we currently have a total of 3 "globally recommended" bladder-sparing treatment options, & notably all of these options are burdened with significant barriers to long-term efficacy success (when compared to bladder removal)....All imo.

Holding tightly...good luck.




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