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Theralase Technologies Inc. V.TLT

Alternate Symbol(s):  V.TLT.W | 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 May 02, 2022 1:58am
185 Views
Post# 34646685

RE:Other Indications Impressive Preclinical Data

RE:Other Indications Impressive Preclinical Data
enriquesuave wrote:

Colorectal preclinical subcutaneous mouse model Rutherin + X-Rays  Vs X-Rays alone.  

Tumor volume after 45 days
Rutherin : 30mm cube. Vs 330mm cube. Thus 90% improvement vs radiation alone

Rutherin survival at 70 days 63% vs 23% for radiation alone 

Excellent improvement for GBM and NSCLC as well. It's in the MD&A on Sedar.  

Enough cash for another 12 months as per report.  Hopefully good data and SP increase before and/or  BTD.


 

In the MD&A, TLT mentions the use of radiotherapy (RT), but they don't specify the type of RT they plan to use in their future GBM & NSCLC studies.  I'm assuming external/x-ray.  However, all of the following RT options are available:  1) only external 2) only internal/intraoperative RT or 3) a combination of the two.  

Based on the various models/graphs depicted in the MD&A, it appears a less durable response was achieved using RT + Rutherrin in an "orthotopic" model vs the subcutaneous & in vitro models, which makes sense if you assume the tumor cells in the orthotopic model are deeper or less accessible to the RT/x-ray beam.  It would obviously be a game changer if they are able to figure out a way to get similar results in humans using only external beam radiation...& the more targeted, less toxic & simpler, the better.  My guess is a standard x-ray(s) wouldn't be enough.  Hope I'm wrong.  All imo.

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