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Theralase Technologies Inc. V.TLT

Alternate Symbol(s):  TLTFF | V.TLT.W

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 Apr 13, 2022 9:50pm
288 Views
Post# 34602527

RE:RE:RE:RE:RE:RE:RE:RE:RE:RE:RE:RE:$tltff The FDA wants an option that has rates better then

RE:RE:RE:RE:RE:RE:RE:RE:RE:RE:RE:RE:$tltff The FDA wants an option that has rates better then
enriquesuave wrote:

If a patient is lying on his back, I suspect that the anterior-superior surface of the bladder may be less in full contact with the drug solution hence, if tumors are found there, they may take up less drug than fully immersed surfaces.  For sure there are probably occasional contractions of bladder to 'stir up' the solution, but just trying to find some potential factors to improve outcomes. Also I hope that evaluate patients who are PR for possible  UTUC early on , so as to not allow potential reseeding of bladder surface from cancer cells migrating from Upper tract to bladder.  That could falsely render a patient NR rather than CR with UTUC confirmed.   These small details may or may not help, but even if we increase 5-10% it makes a huge difference.  I think ultimately we could partner with someone like Merck where they could combo trial TLD-1433 with Keytruda to be used on PR and NR patients.  All IMHO.  Best Single agent in the making and treatment with highest Quality of Life attached.  Among the least amount of side effects and with One single Instillation allows for patient freedom avoidance of multiple painful  invasive visits.  

 

CancerSlayer wrote: The updated protocol/bladder volume calculation (although not perfect) should
help maximize the exposure/surface area of the inner bladder wall.  However, "old" bladders tend to be less expansile & this will pose an ongoing challenge imo.  I imagine over time there will be additional modifications made to help improve dosing, such as what enrique suggested (changing a patient's body position to possibly allow for more even drug distribution...this is done intraoperatively to maximize chemo treatment of certain intra-abdominal tumors that affect the inner lining of the abdomen or peritoneum).  JMO.

 

 


 

Agree...unlike treatment response outcomes, quality of life data is often overlooked or minimized by Big pharma, & yet such data is no less important to patients.  Best single agent in the making & possibly the best combo/adjuvant agent in the making.  Good luck...

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