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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 16, 2024 12:09am
315 Views
Post# 36267521

RE:Best in class 2and 3 year data

RE:Best in class 2and 3 year data
enriquesuave wrote: so far we beat all competitors on 2 and 3 year data and by far.  J&J tar 200 is down to 4.7% at 3 years and we are aiming for 21.4% as per Kaplan Meyer projections so far..  This shows how all other treatments show rapidly declining CR rates once they stop treating.  We also beat 2 years data of recently approved combination treatment Anktiva/ BCG.  24%% vs 25.6% for us based on Kaplan Meyer projection.  Can the FDA give us AA or even full approval right away?


Yep...the K-M projection for 2-3 year data surpasses Keytruda's 1 year results!  The results will certainly speak for themselves.  

A BTD & a load of education/salesmanship need to happen before any shareholder-friendly deal imo.   I'm not sure Big Pharma has a clue about the true potential of our tech as they've been so heavily buried/weighted in favor of chemo & immunotherapy.  Perhaps Dr. Lbiati & our esteemed advisors on the MSAB can help spread the word if/when we have a BTD/AA in hand.  To maximize value in any Pharma deal, one not only needs to back up that value with science, but also with potential for better/broader PDT acceptance in the medical community...shared amongst colleagues & teaching/research hospitals, especially in the US, which holds over 30% of the nearly $5Bn global PDT market (& projected to be over $8Bn in 2033).

If/when we reach the NMIBC approval milestone with our unique PDT compound/approach, our ACT should have a good chance to replace a significant % of this market (i.e. replacing Photofrin, ALA, etc.).  Add in NMIBC, the many other potential indications & widened marketing/acceptance, those billions should grow exponentially. JMO..


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