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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

Bullboard Posts
Comment by Hempdocon Jun 12, 2020 12:24am
170 Views
Post# 31141748

RE:RE:A New Cancer Treatment.

RE:RE:A New Cancer Treatment.
Eoganacht wrote: The same company whose phase 2 pancreatic cancer treatment put Harry Reid into remission are conducting a phase 2 trial for  BCG-unresponsive NMIBC. This company, (ImmunityBio), received fast track designation from the FDA in 2017 for the use of their drug N-803 in combination with BCG for BCG-unresponsive NMIBC and they received breakthrough therapy designation in December 2019.

Preliminary Results: 62 patients have been enrolled to date on this trial with 35 patients with CIS (cohort A) and 27 patients with papillary tumor only (cohort B). In cohort A, of 18 evaluable patients, 16 (89%) have achieved CR. In cohort B, of 13 evaluable patients, 10 (77%) demonstrated no disease at their 3-month and 6-month assessment. Of the 8 patients evaluated beyond this time point, no recurrences have been noted. Three treatment-related adverse events (AEs) were reported (infection, anemia, and bacteremia) ranging grades 2-3. None of the patients experienced immune-related AEs.

QUILT-3.032: A Multicenter Clinical Trial of Intravesical Bacillus Calmette-Guerin (BCG) in Combination With ALT-803 in Patients With BCG Unresponsive High Grade Non-Muscle Invasive Bladder Cancer (NMIBC)

In 2020 they plan to run trials for triple negative breast cancer, lung cancer, head and neck cancer, Merkel cell carcinoma and glioblastoma.

Their treatment is a lot more complicated than TLT's:

"All patients treated in the study will receive via a urinary catheter in the bladder, BCG plus ALT-803 weekly for 6 consecutive weeks (initial induction treatment period). After the first disease assessment, eligible patients will receive either a 3-week maintenance course or a 6-week re-induction course (second treatment period) at Month 3. Eligible patients will continue to receive maintenance treatment in the third treatment period at Months 6, 9, 12, and 18. The study duration is 24 months."

Estimated completion date: January 2023


skys1 wrote: I'm watching Fox Business News. They just had a lengthy segment on a "breakthrough" cancer treatment that cured Harry Reed(former Dem head of the US Senate) of pancreatic cancer. 
We all have this natural killer cell that as part of our immune system attacks, kills, germs, inflammions and such. However cancer T cells have a way to hide from it. They have found a way to re-engineer this killer cell to attack and kill cancer T calls. They expect  this new breakthrough which works on all cancers to revolutionize cancer treatments.
The point of all this is the inept management of Theralase better get "on the stick with their Act or they(and us), will be left behind. 





Thanks Eoganacht...

I had referred to N-803 a while back as another potential competitor, but only as a combo or neoadjuvant form of immunotherapy (i.e. being given with BCG, modified BCG, checkpoint inhibitor or other therapy). 

The downsides are fairly obvious...1).  Like with many immunotherapies, it will likely be restricted to combo/neoadjuvant use. 2). It is highly dependent on the "immune health" of the individual, which certainly is not a given in the elderly patient. 2).  Manufacturing cost.  3). Requires multiple rounds of expensive treatments in combination (the drug doesn't stick around in the body too long, at least not at therapeutic levels) & because of #3....4).  Treatment period never ends (intermittent treatments lasting beyond 18 months post the initial induction treatment).

Guess I just argued myself out of this being a competitor ; ). Good luck...
 

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