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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 Maceron Sep 03, 2019 12:35pm
164 Views
Post# 30090774

RE:RE:RE:RE:RE:CANCER wellness Article on Photodynamic Therapy

RE:RE:RE:RE:RE:CANCER wellness Article on Photodynamic Therapy
toade1313 wrote: If in fact the 1st patient has not been treated because they are waiting for the REB approval on the improved device, it was very misleading to state in the June 27th press release that patients 'could be treated' with the existing device. IMHO 

The amended CTA was submitted to Health Canada to update the current CTA, for an optimized design of the TLC-3200 medical laser system ("Study Device") and is subject to Investigational Testing Authorization ("ITA") by Health Canada and Review Ethics Board ("REB") approval by each Study II site before being used in the Phase II Study. The amended CTA will not impede the Phase II Study as patients will continue to be treated with the Study Drug and Study Device under the current CTA, ITA and REB approvals until the Company receives the new ITA and REB approvals.
Read more at https://stockhouse.com/news/press-releases/2019/06/26/health-canada-approves-amended-clinical-trial-application#AfvTTJmHzeUz7GKj.99

No reason to think anything else at play. And I doubt they would wait on the technology as well given the results acheived to date with the laser prior to modification.
Macer
Bullboard Posts