Join today and have your say! It’s FREE!

Become a member today, It's free!

We will not release or resell your information to third parties without your permission.
Please Try Again
{{ error }}
By providing my email, I consent to receiving investment related electronic messages from Stockhouse.

or

Sign In

Please Try Again
{{ error }}
Password Hint : {{passwordHint}}
Forgot Password?

or

Please Try Again {{ error }}

Send my password

SUCCESS
An email was sent with password retrieval instructions. Please go to the link in the email message to retrieve your password.

Become a member today, It's free!

We will not release or resell your information to third parties without your permission.

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 99942Apophison Oct 18, 2023 5:22pm
387 Views
Post# 35689908

RE:RE:RE:RE:RE:RE:tradeable warrants

RE:RE:RE:RE:RE:RE:tradeable warrants
Eoganacht wrote: The interim trial results are far from "so so"

Keytruda was approved by the FDA  for NMIBC with a durable complete response rate of 18%
Adstiliadrin was recently approved by the FDA with a a durable complete response rate of 23%
Our current (but steadily improving) interim durable complete response rate of 33% along with the absence of trial-related adverse events makes 2-treatment Ruvidar PDT  the best in class stand-alone treatment for BCG-unresponsive NMIBC. We don't need 100% efficacy in order to save many more patients lives and make us all rich.

There is no "insistence" on using the laser to activate PDCs

Nobody is insisting on anything. The technogy is just not ready yet and there may still be obstacles to overcome. Some of the issues and proposed solutions of x-ray activated PDT are outlined in Dr. McFarland and Dr. Lilge's recent paper: https://stockhouse.com/companies/bullboard?symbol=v.tlt&postid=35608406

"Using the laser beam" is not like using the paint brush.

Any cancer cells which escape immediate destruction should be taken care of by the patients own immune system since Ruvidar PDT induces immunogenic cell death.

bigkagan wrote: IMHO, their "so so" trial results so far stem from their insistence on using the laser to activate PDCs in the cancer cells. The laser beam misses lots of cancer cells in the top layer and pretty much all the cells in the lower layers. Using the laser beam is like using the paint brush - some spots always are left untouched. The x-rays are much more effective because they zap all the cancer cells. If I were a patient, I would demand an x-ray instead of a laser



In addition one can't make changes to a clinical trial already in progress, use of a different trigger device in my understanding would have to be done in a new trial. Please correct me if wrong. 
<< Previous
Bullboard Posts
Next >>