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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 Eoganachton Dec 01, 2022 12:25am
723 Views
Post# 35141941

BioTuesdays by Kilmer Lucas

BioTuesdays by Kilmer LucasResearch Capital: Theralase bladder cancer data trending ahead of Keytruda

November 30, 2022

Theralase Technologies (TSXV:TLT; OTCQB:TLTFF) released updated interim data from its Phase 2 pivotal trial with its key value driver, TLD-1433, activated by its proprietary TLC-3200 medical laser system, that Research Capital said looks better than any drug candidate for BCG-unresponsive non-muscle invasive bladder cancer (NMIBC).
 
“If this trend continues, we believe TLD-1433 would be better than Merck’s Keytruda for treating NMIBC,” writes analyst Andre Uddin, Ph.D.
 
Theralase is enrolling 125 patients with BCG-unresponsive NMIBC at 12 clinical sites in North America in its Phase 2 pivotal trial. The latest data was based on 54 patients, of which 43 were evaluable, and represents the sixth clinical set released to date.
 
Dr. Uddin said Merck’s Keytruda achieved a 39% complete response at 90 days and a 19% CR at 12 months in the pivotal KEYNOTE-057 trial.
 
In the Theralase data, 53% of the 43 evaluable patients had a complete response with TLD-1433 at day 90. In addition, at day 360, 29% of 34 evaluable patients had a complete response using TLD-1433 and at day 450, 28% of 29 evaluable patients had a complete response using TLD-1433.
 
“We believe this data indicates that TLD-1433 has the potential to achieve better complete response and longer duration of complete response than Keytruda,” Dr. Uddin said.
 
In terms of safety, eight of the 51 patients reported serious adverse events. Most issues were resolved and Theralase believes these adverse events were not drug related.
 
“All complete response and indeterminate response patients as of the results disclosed today were cancer free according to cytology analysis,” Dr. Uddin said. “Clean safety and promising efficacy makes this one of the most promising NMIBC treatments.”
 
He maintained a “speculative buy” rating on Theralase but lowered his price target to 80 cents (Canadian) from $1.20 as he pushed out his launch date assumption to 2026. The stock closed at 30 cents on Nov. 29.
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