Theralase Submits Authorization for Approval of Anti-Cancer Technology

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The advancement of medical technology is dependent upon seemingly countless clinical studies and investigational testing. The safety of participants and the potential effectiveness of new technologies are always a primary concern. In order for research and testing to happen, particularly in the area of cancer treatment, a number of approvals must be in place to ensure the humane treatment of those volunteering. Theralase Technologies Inc. (TLT:CA) (TLTFF) is one such company going through the various approval channels in order to move forward with their innovative anti-cancer technology.

Theralase submitted an Investigational Testing Authorization (ITA) to Health Canada for approval of its anti-cancer technology, the Theralase TLC-3200 Oncology Laser System. The company’s submission of their ITA follows their recent announcement of a Clinical Trial Application. Theralase is also pending approval from the UHN Research Ethics Board.

One Step Closer to Cancer-Free

Detailed in Theralase’s ITA, by activating their Oncology Laser System with the company’s lead Photo Dynamic Compound (PDC), TLD-1433, the company plans to eliminate Non-Muscle Invasive Bladder Cancer (NMIBC). Each year in the United States, 50,000 men and 16,000 women are diagnosed with bladder cancer – making authorization approval of the Theralase TLC-3200 Oncology Laser System a pivotal moment in the fight against cancer.

“The submission of an ITA to Health Canada for NMIBC is yet another advancement for the Company in its quest to prove the safety, tolerability and efficacy of its anti-cancer technology in the destruction of NMIBC,” said Theralase’s President and CEO Roger Dumoulin-White. “Pending approval of the CTA, ITA and REB, UHN will commence enrolling and treating patients afflicted with this deadly disease.”

Theralase specializes in the design and manufacturing of laser technology that eliminates pain, accelerates tissue healing, and localizes cancer cells in order to accurately and completely eliminate them. Approval from these organizations will allow Theralase to conduct a crucial Phase Ib clinical study that will test the safety and tolerability of the anti-cancer technology on patients diagnosed with NMIBC.

For more information about Theralase’s medical research and development, visit

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