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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

Post by N0taP00pon May 15, 2023 8:41pm
384 Views
Post# 35449427

More options for BCG resistant NMIBC ?

More options for BCG resistant NMIBC ? From cancercommons.org (2020)

Newly emerging treatment options for NMIBC include:
 
A new version of BCG, still in development, called VPM1002. Clinical testing suggests it is effective in more than half of patients who have no response to standard BCG.
A gel form of mitomycin, UGN101. The FDA recently granted a priority review designation to this drug for low-grade NMIBC. In a clinical study, 59% of patients with recurrent cancer achieved complete response, and 84% of them have not experienced a recurrence within a year.
A new, viral-based version of interferon (immune cytokine), called nadofaragen firadenovec (Instilidrin). While interferon is not used very much these days, nadofaragen firadenovec produced durable responses in 53% of patients with high-grade NMIBC that did not respond to BCG treatment.
Of course, the biggest news for NMIBC is the recent FDA approval of the immune checkpoint drug pembrolizumab (Keytruda) for systemic (intravenous) treatment of high grade NMIBC that is not responsive to BCG. In clinical testing, 41% of patients experienced complete responses with median duration of 16 months.
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