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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 Gustoeson Jan 16, 2015 10:47am
116 Views
Post# 23327646

RE:RE:Go go gadget TLD1433

RE:RE:Go go gadget TLD1433
silverT wrote: What do you mean by this "Merck might be interested in ensuring they maintain this market. Since they'll be making TLD1433 (via Sigma Aldrich) maybe they'll take a look. " , Don't we have an exclusive on TLD1433



TLT owns the full rights to the PDC/TLD1433
Sigma Aldrich hired by Theralase to manufacturd the PDC's
Shortlyafterwards, Merck bought Sigma Aldrich for 17B
So technically,,, Merck is manufacturing the compounds for TLT
Merck also has a lot of strategic plans for exploring emerging sciences/treatments/drugs/medical technologies.... so the suggestion is that they might take notice.

 SAFC will develop the Standard Operating Procedures (“SOPs”) to manufacture initial quantities of each of Theralase’s four lead PDCs. Once Theralase selects the final lead PDC at the end of the fourth quarter 2014, SAFC will manufacture both a 100-gram pre-Good Manufacturing Practice (“pre-GMP”) batch and finally a 500-gram GMP batch of the PDC. This final 500-gram batch is intended to be suitable for final sterilization and packaging into individual patient doses for safety and efficacy evaluation through a Health Canada / FDA Phase I/IIa clinical trial
Bullboard Posts