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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 Eoganachton May 31, 2022 4:31pm
224 Views
Post# 34721244

RE:RE:RE:RE:RE:RE:RE:RE:RE:88% demonstrate that CR at 180 days, 69% at 270 days

RE:RE:RE:RE:RE:RE:RE:RE:RE:88% demonstrate that CR at 180 days, 69% at 270 days Good post CancerSlayer. Here's a question I'm not sure anyone has an answer to. Were any of the 12 undertreated patients CR at 450 days? If not, shouldn't the 5 out 20 CR at 450 patients (25%) really be considered 5 out of 8 CR patients (62.5%) as only 8 of the 20 really had a fair shake at becoming CR?

CancerSlayer wrote:

Great news!

 What stood out to me the most & the most meaningful info. imo for the first 20 treated (of which 12 were significantly undertreated) is the following:

There was a 25% CR rate at both the 360 & 450 day assessments.  

The 25% CR rate represents a "minimum" CR rate considering there are PR patients yet TBD (3 patients at 360 days & 2 patients at 450 days).  This minimum 25% CR rate already beats the approved competition (Keytruda at 19% & Valrubicin at 17%) & is in very good standing with the rest (12 month CR for Nadofaragene = 24%, Oportuzumab = 17%, Atezolizumab = 25%, N-803 + BCG = 40%;  the latter obviously requires BCG which is in short supply & also requires a minimum of "18" intravesical treatments, which can lead to patient compliance problems).  Additionally, maintaining a 25% CR rate (at 360 & 450 days) at this later stage post-treatment could signal a type of minimum (or near-minimum) durable response threshold where the percent likelihood of a patient maintaining a CR after a certain "late" point may be higher compared to earlier assessment stages....JMO.  GLTA.

 

 

enriquesuave wrote:

 

Can someone post the chart with the 1st 20 patients?  Since 1st 12 were severely undertreated and 5 were wrongly dropped early on ( never got a Maintenance treatment at 180 days)and one patient died of Heart failure from that group, IMO we are looking very good.

 

Rumpl3StiltSkin wrote: Enrique, I am very encouraged. What would really get me going is if we start to see some PR after first dose convert to CR after second dose. THAT would be huge! IMO... It would show the market that trying 1433 again is a great idea if it doesn't work the first time.
 

 

enriquesuave wrote:

Actually numbers were better for evaluable patients at 180 days (50% CR)vs (46% CR)at 90 days. That is 109% (not 88%).  They are being conservative.  That is why I'm waiting to see numbers at 270 days which could foretell 360 and 450 days on Optimized patients.  270 days is steady at 39% CR meaning no new data in last month.  Next update will show what a second treatment can do in Optimized patients who were NR or PR at 180 days.  In the new MD& A released today, the 1st 20 patients chart with all assessments completed shows very good numbers and these include the 1st 12 non-Optimized.  If BTD is granted, which it definitely should IMO, and we show consistent data or even better, on a few more patients ( all Optimized) , then AA is next.  IMHO.

 

FGPstock wrote:

I think you guys may be reading this statement wrong. 46% were CR after 90 days. then 88% of the 46% were still CR after 180.

Not sure how the PR factors in


For all Evaluable Patients, who achieved a CR at 90 days88% demonstrate that CR at 180 days, 69% at 270 days, 50% at 360 days and 56% at 450 days, demonstrating a strong duration of complete response.

 

 


 

 




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