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Theralase Technologies Inc. V.TLT

Alternate Symbol(s):  V.TLT.WT | 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 ScienceFirston Dec 06, 2022 11:07pm
285 Views
Post# 35155157

Patients discrimination with immunotherapy drugs

Patients discrimination with immunotherapy drugs Below is the perfect example of where TLT has a huge benefit over immunotherapy drugs. 

For example, it would confer TLT a 4x greater pool of patients over Keytruda in the BCG-unresponsive because our drug doesn't test for specific genetic profiles.  That's another key attribute that could make us very attractive to a big pharma as it equals to higher revenues.

Check this example (from another type of indication - NSCLC):

Adagrasib, given in tandem with Keytruda, shrank tumors in 49% of 53 patients with newly diagnosed KRAS G12C-mutated non-small cell lung cancer (NSCLC) in a phase 2 trial, according to data to be presented at the ESMO Immuno-Oncology Congress 2022. The combo also showed relatively low liver toxicity, relieving a major safety concern.

Based on the phase 2 results, Mirati is moving the adagrasib-Keytruda regimen into phase 3 testing in front-line NSCLC soon. The company met with the FDA in September, and the agency has agreed with the trial design, Meek said. The phase 3 will only enroll patients with low PD-L1 expression, he said.


And despite the efficacy numbers below, Mirati is the subject of big pharma takeover.  Mirati is worth 4.2B$US.


The adagrasib-Keytruda pairing delivered the 49% overall response rate after investigators followed 53 patients for a median 3.5 months.

Mirati is once again the subject of Big Pharma takeover talks: report


Bloomberg reported Tuesday that Mirati Therapeutics is once again the subject of takeover talks, reviving similar rumors from a year ago. In fact, Mirati has been considering strategic options “for some time,” according to the latest reports. 

No formal bids have been proposed, according to Bloomberg, which claimed that the cancer-focused company is working with an advisor and larger pharmas are considering the “merits of a transaction.” Notably, the report said that a deal doesn’t appear to be imminent.

A spokesperson for Mirati said the company would not comment on speculation. 

The latest reports come as the company prepares to challenge Amgen’s KRAS inhibitor packleader Lumakras with its own competitor, adagrasib. The drug is currently being reviewed under the FDA’s accelerated approval program with a December 14 decision deadline. 


Dec. 5, 2022:

Mirati Therapeutics Presents Late-Breaking Results Evaluating Concurrent Adagrasib and Pembrolizumab in First-Line Advanced/Metastatic Non-Small Cell Lung Cancer (NSCLC)

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