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Destroying Cancer at the Speed of Light®

Clinical Study Underway (68 of 100 Patients Treated)
Expected to complete enrollment at the end of 2024
Expected to complete study at the end of 2026


Bullboard - Investor Discussion Forum Theralase Technologies Inc. V.TLT

Alternate Symbol(s):  V.TLT.WT | 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... see more

TSXV:TLT - Post Discussion

Theralase Technologies Inc. > Ph 1b patients #5 and #6 still cancer free after 2 years
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Post by ScienceFirst on Jun 22, 2022 9:05am

Ph 1b patients #5 and #6 still cancer free after 2 years

« … with patients five and six demonstrating CR with no presence, recurrence or progression of the disease at up to 24 months post treatment."

All this, with one dose!

The holy grail of oncology; 

- high efficacy,
- low number of treatments (1 in our case)
- no side effects,
- total destruction of the late-stage solid tumor.

You cannot ask for anything better than that.
Comment by Infinity on Jun 22, 2022 10:11am
Science First, I get your point. Loud and Clear. 1. I am perplexed by the market valuation at $ 0.30 +/_ for many years now. 2. The big pharma companies are ignoring TLT for a reason. Or the Management is not disclosing the interest shown by Big Pharma. Or even worse, the Board is trying to ignore the Interest of the Share holders.
Comment by langosta on Jun 22, 2022 11:11am
Surely big pharma would not be deliberately suppressing our market value over these many years by any of the various means available to them.  Why that would be positively criminal, and we all know that big pharma are so squeaky clean that they would never stoop to such shenanigans. https://violationtracker.goodjobsfirst.org/industry/pharmaceuticals
Comment by ScienceFirst on Jun 22, 2022 11:47am
Langosta ... It's all about market shares. Whether you're TESLA, AMAZON, MERCK, GOOGLE, FACEBOOK, etc ... You're the CEO of a big pharma and have stock options.  Why would you let an opportunity run away?  Why would you let a competitor shift you? TLT had its Ph. 2 to do.  It won't even be completed until 2025.  What was the rush for those big pharmas, when ...more  
Comment by langosta on Jun 22, 2022 12:47pm
I know it's all about market share. As far as large corporations are concerned that can often be described ib one word, "Greed" or perhaps, "Ego". After all, who gets hurt when a company is caught in some impropriety? CEO's, Company Boards, Directors? I don't think so. As long as  the company can claim "Personhood" then it's the company that pays ...more  
Comment by ScienceFirst on Jun 22, 2022 12:53pm
Langosta ... Again, you're the CEO of a big pharma and have stock options.  Why would you let an opportunity run away?  Why would you let a competitor shift you?
Comment by ScienceFirst on Jun 22, 2022 11:37am
Infinity ... Quite possible that it's rather TLT that asked big pharmas to come back later when more Ph. 2 data is out.  When you have something you know everyone will want, that's the position you usually take.  You wait till the data is undisputable so you can have the best position when negociations come.   And I saw this for a biotech that was bought for 30B$US in ...more  
Comment by skys1 on Jun 22, 2022 11:46am
As I have posted several times before. TLT management is not business stupid. They know when they have commercialization approvals in hand, TLT will be worth far more than it's current valuation. Hence, no negotiations until BTD & AA are in hand which should be only several months away, then they will get down to some serious business. Then we will see a more viable valuation. It is surely ...more  
Comment by enriquesuave on Jun 22, 2022 10:45am
Pretty awesome results  I suppose the FDA will see the same level of detail patient per patient as in article.  The potential Gold Standard statement by Dr Mandel makes sense if we can continue to demonstrate a high level of durable efficacy with 2 simple safe treatments.  Much less burdensome for patients and hospitals as well  IMhO  
Comment by ScienceFirst on Jun 23, 2022 8:51am
In fact, both ph. 1b patients #5 and #6 have now reached their 3y+ milestone, as we speak, as the statement below was dated of August 2021 and that p#6 reached 540 days on Sept. 30, 2019, so initially treated around April 8, 2018. It's impossible that the FDA pass over such a treatment and not grant us Breakthrough designation and Accelerated Approval program, especially that this is for a ...more  
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The Road to Saving Lives: Clinical Study Underway

  • Clinical Study with 68 of 100 Patients Treated (Enrollment to be completed by end of 2024, with study completed by end of 2026)
     
  • Ground Floor Investment Opportunity in Multi-Billion Dollar Industry
     
  • Best-in-class treatment for NMIBC (according to interim clinical data)
     
  • NMIBC (Non-Muscle-Invasive Bladder Cancer)
     

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Toronto, ON M4B 3G4
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Local Phone:
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