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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 May 15, 2023 4:26pm
240 Views
Post# 35448995

RE:RE:What's Next?

RE:RE:What's Next?

enriquesuave wrote:
Eoganacht wrote:
Given the stability of CRs after the 180 day assessment, and taking into account only patients who were CR at both their 90 day and 180 day assessments I think we can be confident that:
 
90 days from now we should be at a 450 day CR rate of 31%
(12 out of 39 should be CR)
 
180 days from now we should be at a 450 day CR rate of 34%
(14 out of 41 should be CR)
 
270 days from now we should be at a 450 day CR rate of 40%
(19 out of 47 should be CR)
 
Stellar results. And this includes the 12 undertreated patients.

Nice Eoganacht.  Without 12 undertreated patients we would may e be looking at 50-55% 450 CR rate Imo. With only 2 treatments. I can imagine that NR and IR patients will eventually be given 3-4 treatments and perhaps we get another 10-20 % increase in CR rate perhaps? 


 

Yep Enrique...

If our ACT is approved (have little doubt in my mind), clinicians will have the option to add a treatment(s) as they see fit for the more resistant/highly pre-treated patients...this is the art of medicine, which is unfortunately fading in general medicine & other specialties.  Regardless, practice guidelines are just that...guidelines.  They are not hard & fast rules.  

Based on data trends thus far, I'd consider an NR to generally not change if a patient remains NR 3 to 6 months after the 2nd treatment.  Perhaps this subset of patients could receive 1 to 2 additional treatments ~3 months after the 2nd treatment...& perhaps additional treatments could be given more frequently (i.e. 3 months apart instead of 6)?.... JMO.  Our ACT should also more easily accommodate other treatments if needed (in combo or in series), simply based on the fact that we are a 2 treatment protocol that has few significant adverse effects.

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