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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 CancerSlayeron May 15, 2022 1:26am
284 Views
Post# 34684547

RE:RE:Final clinical results of N-803 BCG Unresponsive NMIBC Trial

RE:RE:Final clinical results of N-803 BCG Unresponsive NMIBC Trial
enriquesuave wrote:

Same results as before.  Very good, but it's also a combination therapy  2 drugs will always work synergistically and give added efficacy.  TLD-1433 single agent should give us results very close to those IMO after full trial results, but we will be 1 single treatment vs 15-21 instillations.  All IMHO 

 

Eoganacht wrote:  were presented at the AUA2022 yesterday, Friday, May 13. We already knew the results - Cohort A  (83 patients with CIS) achieved - 71% CR at any time - 36% CR at 2 years.  Cohort B (77 patients with papillary disease) achieved a disease-free survival rate of 57% at 12 months and 48% at 24 months.

Final Clinical Results of Pivotal Trial of IL-15R&[alpha]Fc Superagonist N-803 with BCG in BCG-Unresponsive Non-Muscle Invasive Bladder Cancer (NMIBC) CIS and Papillary Cohorts

 

 


 

If we achieve similar efficacy with only two required treatments vs 15+, that'll be a no-brainer.  Also, the BCG shortage has precluded its use in many urologic practices & a restricted supply will generally drive prices higher.   Imo, docs will continue to look for other options that are more feasible/practical for both their patients & busy practices.  If FDA approved, TLT's more simplified single-agent/two-treatment option should provide stiff competition against any immunotherapeutic or chemotherapeutic combo therapy.  

And it's not a far stretch to think that an additional treatment of our ACT (if needed) or if used in combination with chemo or an immunotherapeutic could very well surpass any other combo option.  

Another area that warrants further study is figuring out the best method to maximize delivery of an intravesical drug.  Imo, the primary efficacy-limiting factor with our ACT is most likely attributed to less-than-maximal drug/light absorption...not the mechanism of its cancer cell destruction.  I expect our ACT will eventually reach even higher heights once this limiting step in our intravesical treatment protocol is further perfected.  We already learned that maximizing bladder volume (increasing pressure) logically increases drug absorption & hence efficacy.  All imo.  GLTA.

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