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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 Sep 02, 2021 9:58pm
224 Views
Post# 33807889

RE:RE:Uddin's Comments on Buy rating

RE:RE:Uddin's Comments on Buy rating
CancerSlayer wrote:

 

Kingpin68 wrote:
For the 27 subjects in TLTs pivotal trial to achieve the same CR rate at 360 days as Keytruda, an additional three subjects out of the 11 which had not received both doses of TLD-1433 would need to achieve CR representing a 27 per cent threshold (3/11) we believe this is a feasible threshold for Theralase given the data presented to date, Uddin said... As the Phase 2 pivotal trial continues to progress, we believe the results should elucidate the efficacy potential of TLT-1433. We are maintaining our SPECULATIVE BUY rating and a target price of $0.70, Uddin wrote.

 

 

The number of patients who had not received two doses at the 270 & 360 day marks would be 9 of the 27 total reported (not 11).  The 270 & 360 day marks represent the % of patients who still have their data pending....the interim marks have nothing to do with the number of patients who have yet to receive their 2nd treatment.  Patients 13, 14 & 15 all received their 1st treatment before 2/24/2021.  So we have 3 patients from Ph 1b & the 15 patients from Ph 2 (a total of 18 of 27 patients) who would have received two treatments by now (at 0 & 180 days).  The 27% threshold doesn't change, but we only need 3 of the remaining 9 to be CR at 360 days...all of whom will have received "two" optimized treatments.  That would put us well above that 27% threshold.  

I also maintain a STRONG SPECULATIVE BUY, but I won't dare try to put a target price on this one ; )
JMO.  GLTA.


 

Sorry folks...meant to say the 27% threshold does change...it would be 33% for the remaining 9.  Discard the highlighted statement...should have read "That would put us safely above Keytruda's 19% threshold".  Ugh...back to sleep.

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