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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 enriquesuaveon Apr 27, 2021 4:56pm
212 Views
Post# 33076751

RE:RE:RE:wow, what a great day....

RE:RE:RE:wow, what a great day....

"In accordance with FDA guidelines to industry, the patients who have achieved a PR are being further assessed via CT scan and biopsy of the prostatic urethra to determine if upper tract Urothelial Cell Carcinoma (“UCC”) or prostatic urethra UCC can be detected to allow these patients to be re-categorized as CR."
Hope we get clarification on those 2 patients and pray that they come out CR.


enriquesuave wrote:

For the next report, it would be good to see the 3 months data for all pending patients and partial responders final confirmation as well as 9 months data ( 3 months after 2nd treatment).  We were just given data after one single treatment which is 3 and 6 months.  After 2nd treatment I hope we see all those CR maintaining CR status at 9 months and possibly a few more others become CR.

 

enriquesuave wrote: I don't know what the market expected, but we knew that we would only get the same data as last Q  report plus patients 13-15. So far the treatment is showing at least 6 months durability just when patients will get treated a second time with an optimized treatment.  As for 13-15 so far 2 out of 3 are CR. Not bad.  Just need more data, and even if we just get good news from those pending and maybe clarify the partial responders, then market will have a better idea of  efficacy potential. We are still negatively affected by the under treatment of the first set of 12 and not enough new data. IMO

 

 



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